Health & Beauty Product Recalls

This recall involves Hepo-branded adult portable bed rails, model 110039. The recalled bed rails have white tubing with black foam rubber handle grips, a black fabric pouch, and measures about 16 inches wide by 25 inches high. The model number is located on the original product packaging.

This recall involves Arey, Bari Life, Bird&Be, Biote, Dr. Fuhrman, NuLife, HMR, Bariatric Pal, Noevir, Zenbean and Sakara brand iron-containing dietary supplements without child-resistant packaging. Brand / Product Name Arey Not Today, Grey (60ct and 180ct) 0034I5 Sept. 2027 860007168901 0342B5 Feb. 2027 860007168901 0342B5A Feb. 2027 860007168901 0360G5 July 2027 860007168901 0442H4 Sept. 2026 860007168994 0442H4A Sept. 2026 860007168994 0442H4B Sept. 2026 860007168994 0483G5 July 2027 860007168994 Bari Life Complete Bariatric Vitamin - Watermelon (60ct) 0138G5 July 2028 860012913930 0177D3 April 2026 860012913930 0207A4 Jan. 2027 860012913930 0333K4 Nov. 2027 860012913930 Bird&Be The Prenatal Essentials for Females (30 pkts) 0005K4 Oct. 2026 860010126417 Bird&Be The Power Prenatal for Females (30 pkts) 0006K4 Aug. 2026 860010126479 Bird&Be The Power Prenatal for Females + CoQ10 Boost (30pkts) 0060L4 Aug. 2026 860010126493 Bird&Be Female Fertility Power Prenatal Pack (30 pkts) 0346C5 March 2027 860013460136 0354F5 May 2027 Bird&Be Complete Prenatal Pack (30 pkts) 0342C5 May 2027 860013460174 0345F5 0345F5A 0345F5B Bird&Be Female Fertility Power Prenatal + CoQ10 Pack (30 pkts) 0360F5A June 2027 860013460143 0360F5 June 2027 0350C5 March 2027 Biote Nutraceutical Iron+ (30ct) 0068F5 May 2027 0516K4 0516K4 Jan. 2027 0068F5 Dr. Fuhrman Gentle Prenatal Multivitamin + D3 (120ct) 0091A5 Feb. 2027 829584500061 Dr. Fuhrman Pixie Vites Children's Multivitamin (120ct) 0130K4 Dec. 2026 829584500153 NuLife Advanced Bariatrics Multivitamin Chewable Tablets (60ct) 0041C4 Feb. 2027 746888915028 0248J4 Oct. 2027 746888915028 0248J4A Oct. 2027 746888915028 0305F5 July 2027 746888915028 0342J3 Oct. 2026 746888915028 0363F3 June 2026 746888915028 0363F3A June 2026 746888915028 0416C5 April 2027 746888915028 0440H4 Sept. 2027 746888915028 0521D5 May 2027 746888915028 HMR Multi Daily Vitamin and Mineral Supplement (60ct) 0013H5 July 2027 00709355144413 Bariatric Pal Ultra Multi Bariatric Multivitamin (90ct) 0148I4 Sept. 2026 0038407566232 Noevir Inner Care Premium BioEssentials (120ct) 0134F4 July 2026 N/A Zenbean Kids Café Instant Coffee + Nutrition Latte, Original, Caramel, Chocolate, and Vanilla (30srv) 0028H4 Aug. 2026 810067444910 0051H5 Aug. 2028 850067341338 0052H5 Aug. 2028 850067341314 0050H5 Aug. 2028 850067341321 Sakara The Foundation (30pkts) 0340A5 Sept. 2026 858151008334 0340A5A Sept. 2026 858151008334 0340A5B Sept. 2026 858151008334 0340A5C Feb. 2027 858151008334 0340A5D Feb. 2027 858151008334 0540H4D June 2026 858151008334 Sakara The Foundation: Prenatal (30pkts) 0338A5A Feb. 2027 858151008341 0338A5B Feb. 2027 858151008341.

This recall involves Mindbodygreen Ultimate Multivitamin+ dietary supplement bottles with the following UPC, lot numbers and manufacturing dates (Month/Year format). The dietary supplements come in eight-ounce amber glass bottles with black caps, each containing 60 capsules. The UPC, lot numbers and manufacturing dates are printed on the bottle. UPC Lot Number Manufacturing Date 850027975177 0515I1 09/2021 0130B2 01/2022 0187I2 08/2022 0324J2 10/2022 0309A3 12/2022 0368L2 12/2022 0272B3 02/2023 850027975429 0408H3 06/2023 0143A4 12/2023 0179C4 02/2024 4021131 05/2024 4033211 07/2024 4080841 10/2024 A010611 03/2025 A021211 03/2025

This recall involves Gagaku-branded ice cream shop toy playsets. The recalled toy set includes 16 wooden pieces: a cash register, three ice cream cones, six scoops of ice cream, four popsicles, and two cupcakes in varying colors or "flavors." It also comes with one plastic credit card, five plastic dollar bills, one plastic menu and a two-level pink display box labeled "ICE-CREAM" on the front, with a black sign on the side. "GAGAKU" and "Model: KABI-0176 G062401IC" are printed on a label on the underside of the toy.

This recall involves "RELIEVE" numbing cream. The cream comes in a short wide-mouthed white container. A label is located on the front with black lettering and "RELIEVE" in large type and the company's logo and "Mad Rabbit", "Numbing Cream" and "Menthol" in smaller type.

This recall involves two types of Bariatric Fusion dietary supplement bottles: high ADEK multivitamin capsules (90 and 270-count bottles) and One Per Day bariatric multivitamin capsules (90-count bottle), both with 45mg of iron. The recalled bottles are white and orange. Only bottles with smooth cap tops that lack the "push down & turn" embossed lettering are included in this recall. The Bariatric Fusion logo is printed on the front of the bottles. Lot number 0066J4, 0065J4, 0453B5 or 0370B5 is printed on the bottom of the bottles.

This recall involves three types of California Gold Nutrition dietary supplements: Daily Prenatal Multi, Ultamins Women's Multivitamin, and Ultamins Women's 50+ Multivitamin. The California Gold Nutrition Daily Prenatal Multivitamin bottles are white with a white lid and a gold border label. The bottle contains 60 fish gelatin softgel dietary supplements. The California Gold Nutrition Women's Multivitamin and Women's 50+ Multivitamin both have dark purple packaging with a gold border label. Both products contain 60 capsules in foil within the packaging. The following batch numbers and expiration dates for the products are printed on the back of the package near the bottom of package/sleeve. Products Batch Codes Expiration Dates Daily Prenatal Multi 2307050A, 2404096A, 2411100A 08/2025, 05/2026, 11/2026 Ultamins Women's Multivitamin V0532, V0533 11/2026, 07/2026 Ultamins Women's 50+ Multivitamin V0534, V0536 07/2026, 11/2026

This recall involves NFH Dietary Supplement bottles for Iron SAP, Heme Iron SAP and Prenatal SAP. The bottles are white with the brand name "NFH" and the firm's logo of a leaf in blue. The date code is on the bottom of the bottle. The recalled dietary supplement bottles have the following description and come in various sizes: Product Name Description Sizes Date Codes Iron SAP Iron Glycinate 60 Capsules (1029U) 120 Capsules (1167U) 60 capsules 5398705/31/2027 5398805/31/2027 5398512/31/2026 5398612/31/2026 5398306/30/2026 5398406/30/2026 N00274 07/31/2025 120 capsules 538975/31/2027 539875/31/2027 539885/31/2027 5398512/31/2026 5398612/31/2026 539846/30/2026 N00274 6/30/2025 Heme Iron SAP (Porcine) Superior Absorption and Bioavailability 60 Capsules (1124U) N00265 - 03/31/2025 53809 - 05/31/2026 53810 - 07/31/2026 57807 - 10/30/2026 53811 - 10/31/2026 57806 - 10/31/2026 62379 - 08/31/2027 Prenatal SAP Multivitamin 180 Capsules (1034U) 5821709/30/2027 5822009/30/2027 5736105/31/2027 5736905/31/2027 5737005/31/2027 5737205/31/2027 5821405/31/2027 5396803/31/2027 5719401/31/2027 5736001/31/2027 5396311/30/2026 5396411/30/2026 5396511/30/2026 5396611/30/2026 5396711/30/2026 5395410/31/2026 5395610/31/2026 5395810/31/2026 5396010/31/2026 5396110/31/2026 5396210/31/2026 5395307/31/2026 5394605/31/2026 5394504/30/2026 N00287 08/31/2025 N00285 04/30/2025 N00284 03/31/2025

This recall involves the Bed Assist Rail with Adjustable Heights (model numbers 7007 and 7057) and the Bed Assist Rail Without Legs (model number 7037). The Bed Assist Rail with Adjustable Heights is made of black or white metal tubing with a rounded black foam rubber grip handle and a fabric pouch. The Bed Assist Rail Without Legs is made of silver metal tubing with a black foam rubber grip handle and a black fabric pouch. There are no model numbers or brand-specific labels on the recalled bed rails.

This recall involves the Hand Bed Rail (model P1410), Hand Bed Rail with Pouch (model P1410-P), Hand Bed Rail with Floor Support (model P1411), and Hand Bed Rail with Floor Support with Pouch (model P1411-P). The name "Essential Medical Supply, Inc." and the model number are printed on a label located on the grip handle of the bed rails. The rails are made of either chrome or white metal tubing and include black padding on the grip handle and under-bed frame. They measure approximately 17 inches to 21 inches high by 20 inches wide. Only bed rails that do not have model numbers ending in "R" are included in this recall.

This recall involves all Capri Blue Deodorizing Pet Bedding Spray, Capri Blue Waterless Foaming Shampoo, Capri Blue Deodorizing Fragrance Spritz and Capri Blue Detangling and Conditioning Spray. The spray bottles are blue and white. "capri BLUE" and the product name are printed on the label.

This recall involves Solaray Liposomal Women's in 60 and 120 count, Solaray Universal Multivitamin in 60 and 120 count, and Solaray Liposomal Women's 50+ Multivitamin in 120 count. The bottles are a clear silver color with white pop top lids. The white label on the front of the bottles displays the Solaray logo, product name, product type and size count. The 60 count bottles are contained in cartons, which are substantially similar in appearance to the bottles inside. All lots are included in the recall. Name Count SKU Solaray Liposomal Women's 60 076280193251 Solaray Liposomal Women's 120 076280339536 Solaray Universal Multivitamin 60 076280640168 Solaray Universal Multivitamin 120 076280830385 Solaray Liposomal Women's 50+ Multivitamin 120 076280154832

This recall involves Ferrous Sulfate Enteric-Coated Tablets dietary supplements containing 324 mg of ferrous sulfate (iron) in bottles of 100 tablets. "Nationwide Pharmaceutical" and its logo are printed on the top left of the bottle's label panel. The recalled bottles include lot numbers M0786, M0816, M0817 and M0818, which are printed on the bottom of the bottle.

This recall involves Screaming Plush Monkeys in brown, blue and pink. The monkeys are 23 inches long and make a scream-like sound when the front paw is pressed. The front paws of the plush monkey have Velcro so that the monkey's arms can be wrapped around a consumer's neck. Model TM-3280 and Diamond Visions, Inc. are printed on a tag on the monkey.

This recall involves two models of Vaunn Medical Bed Assist Rail adult bed rails, model numbers M876N-AAWH-APVM and M876N-SABK-APVM. Model M876N-AAWH-APVM is a rectangular bed rail made of white metal tubing with a black foam rubber grip handle. Model 876N-SABK-APVM is made of black metal tubing with a rounded black foam rubber grip handle and a fabric pouch. The model number is printed on the weight capacity label located on the grip handle.

This recall involves prescription drugs Aprepitant 125 mg capsules sold in cartons containing one blister card of 6 capsules and 5 gram tubes of Lidocaine and Prilocaine cream sold in cartons containing 5 tubes and packed with or without 12 dressings. The Aprepitant capsules are in a non-child resistant blister card packaged in a carton that has the name "Sandoz," the name of the medication, dosage, NDC number, lot number, and expiration date on the carton and on the blister cards. The warnings "This unit-dose packaging is not child-resistant" and "For institutional use only" are listed on the carton. The Lidocaine and Prilocaine cream is packaged in a 5 gram tube with a continuous thread white closure. The name "fougera®," the name of the medication, dosage and NDC number are printed on the carton and tube and the expiration date and lot number are printed on the carton and stamped on the crimp of the tube. The warning "FOR HOSPITAL USE ONLY" is printed on the carton and the tube. Product Description NDC Number Lot Number Expiration Date Aprepitant Capsules 125 mg 0781-2323-68 Carton of 1 Blister Pack of 6 capsules 0781-2323-06 Blister Pack LK3209 LC6454 04/2024 12/2023 Lidocaine and Prilocaine 2.5%/2.5% Cream 5 gram Tubes 0168-0357-56 Carton of 5 tubes and 12 dressings 0168-0357-55 Carton of 5 tubes 0168-0357-05 Tube LA2782 LA2784 LV0667 LX5350 MA1640 MB3205 LA2785 LR9041 MB3209 03/2023 03/2023 02/2024 03/2024 03/2024 04/2024 03/2023 11/2023 04/2024

This recall involves Nova Medical Products Home Bed Rail (Model No. 6093) and Home Bed Rail with Legs (Model No. 6094). The bed rails are made of white metal tubing with a black foam rubber grip handle and removable fabric cover. The model number is printed on a label located on the grip handle and begins with BL6093 or BL6094.

The recall involves Samnyte Tattoo Numbing Cream sold in 60ml and contains Lidocaine 5% with Vitamin E. The product was sold in a white tube with a flip-top closure. The drug facts label is on the back.

The recall involves Mohnark Pharmaceuticals Lidocaine 4% Topical Anesthetic Cream. The product was sold in a white tube with a flip-top closure. Mohnark Pharmaceuticals is printed under the blue and green logo on the right side of the product tube. The lot code is located at the bottom of the product tube. The affected lot codes are 01202201, 210201, 210301, 210503, 210505, 210601, 211002 and 210401. The UPC 860002324906 is located on bottom side panel of the packaging.

This recall involves bottles of Rae Wellness Prenatal and Immunity Capsules. Both products were sold in 60-capsule bottles and contain iron and have "Rae" in yellow lettering and "Prenatal" or "Immunity" printed on the label. The bottles have a white continuous thread closure.

This recall involves Hempväna pain relief products containing lidocaine, including Hempväna Ultra Strength Pain Relief Cream with Lidocaine, Hempväna Ultra Strength Pain Relief Cream Night with Lidocaine, Hempväna Ultra Strength Pain Relief Cream Turmeric with Lidocaine, and Hempväna Pain Relieving Hand & Body Lotion with Lidocaine. "Hempväna" and "Pain Relief" or "Pain Relieving" is printed on the packaging in large black letters. The UPC number appears on the bottom panel of the package. The UPC number for the lotion is on the label on the back of the product. The item numbers and UPC for the recalled products are as follows: Product Name Item No. UPC Description Hempväna Ultra Strength Pain Relief Cream with Lidocaine 15436 97298053542 4 oz. jar with twist-off lid and green and red label Hempväna Ultra Strength Pain Relief Cream Night with Lidocaine 14597 97298052583 4 oz. jar with twist-off lid and green and purple label Hempväna Ultra Strength Pain Relief Cream Turmeric with Lidocaine 14460 97298052170 4 oz. jar with twist-off lid and green and orange label Hempväna Pain Relieving Hand & Body Lotion with Lidocaine 15440 97298053566 8 oz. bottle with pump dispenser and green and red label.

This recall involves the PhysiciansCare brand Extra Strength Non Aspirin, Aspirin, Extra Strength Pain Reliever, Ibuprofen, Medication Station, and Multi-Pack over-the-counter drugs. The products contain aspirin, acetaminophen, or ibuprofen. They are packaged in cardboard boxes of 50, 100, 250, and 500 tablets per box. Product Drug Tablet Amount Extra Strength Non Aspirin Acetaminophen (500 mg) 50 tablets 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Aspirin Aspirin (325 mg) 50 tablets 100 tablets 250 tablets 500 tablets Extra Strength Pain Reliever Acetaminophen (250 mg) Aspirin (250 mg) 100 tablets 250 tablets Ibuprofen Ibuprofen (200 mg) 100 tablets 250 tablets 500 tablets 2 boxes of 100 tablets each Medication Station / Multi-Pack Acetaminophen (500 mg) Aspirin (325 mg) Ibuprofen (200 mg) Antacid (420 mg) 4 boxes of 100 tablets each with outer station 4 boxes of 100 tablets each without outer station The Antacid is not subject to this recall.

This recall involves the Hand Bed Rail (model P1410), Hand Bed Rail with Pouch (model P1410-P), Hand Bed Rail with Floor Support (model P1411), and Hand Bed Rail with Floor Support with Pouch (model P1411-P). The name "Essential Medical Supply, Inc." and the model number are printed on a label located on the grip handle of the bed rails. The rails are made of either chrome or white metal tubing and include black padding on the grip handle and under-bed frame. They measure approximately 17 inches to 21 inches high by 20 inches wide.

This recall involves bottles of LifeSeasons Blood Nourish-R dietary supplement with iron. The brown, 60-capsule count bottles, have a white and red label, with the LifeSeasons logo printed on the front and the UPC code 853760002452 on the back. The following lot number and corresponding expiration date are printed on the underside of the bottle: Lot Numbers Expiration Dates 06242008 8/23 03262012 10/23 06242007 10/23 06242021 11/23

This recall involves Welmate Lidocaine Numbing Cream in a 113 g (4 oz.) white jar with a blue, orange and green label and a white cap. "Welmate," "5% Lidocaine," the Welmate logo and UPC code 373581105045 or 373581000012 are printed on the label. The lot numbers and corresponding expiration dates included in the recall are printed on the underside of the jar as follows: Lot Numbers Expiration Dates ELNC2001 05/2022 ELNC2002 05/2022 EL5C2001 11/2022 EL5C2002 11/2022 EL5C2101 11/2022 EL5C2102 11/2022

This recall involves Scalpa Numb Maxium Strength Topical Anesthestic Cream in a 10 gram black and white tube with a white cap. "SCALPANUMB" and "Maximum Strength Topical Anesthetic Cream" are printed on the label. The expiration date is marked as EXP 202307 on the crimped end of the tube. Batch number 1000000101, Code: C1 and the UPC code 857076008689 are printed on the outside of the box.

This recall involves The Vitamin Shoppe's Vthrive Bioactive Women's One-Daily Multi vitamins. The 60-count capsules were sold in an amber bottle with a gray top. Vthrive and Bioactive Women's One-Daily Multi are printed on a blue label on the bottle. Item number VS-6104 can be found on the back of the bottle and lot number 006218, 006454, 006495 or 006779 on the bottle's underside. Only the 60-count bottles are included in this recall.

This recall involves The Vitamin Shoppe's Energy Formula multivitamins in a white bottle with a blue, white, and gold label. Each bottle contains 90 tablets and has the code VS-3293 with the lot number 8102351 located on the bottom of the bottle.

This recall involves NumbSkin pain relief cream with 5% lidocaine. The topical anesthetic cream was sold in 30 grams in a white with blue tube. NumbSkin is printed on the tube. Lot 9238 and a date code of 10/2019 through 09/2020 in a MM/YYYY format is embossed on the tub's thin end. Batch number 9238 is printed on the product packaging.

This recall involves TriDerma Pain Relief Cream with 4% Lidocaine in a jar and tube. The 4 ounce jar is white with a lime green and pink printed label and has a white dome cap. The 2.2 ounce tube is white with a lime green and pink printed label. The lot numbers and expiration dates of the affected products can be found on the bottom of the jar and on the front of the crimped end of the tube. "TriDerma Pain Relief Cream" is printed on the jar and tube. Lot Number Expiration Date 21088 04/2021 20189 04/2021 0738F02A 06/2021 0738F04A 06/2021 0738F04B 06/2021 0738F04C 06/2021 0739A22A 01/2022 0739A22B 01/2022 0739A23A 01/2022

This recall involves Numb 100 Topical Anesthetic Cream. The recalled cream is in a 1.35 fluid ounce white jar with a rounded cap. Numb 100 Topical Anesthetic Cream and a blue cross are printed on the jar's front panel.

This recall involves Women's Iron Complete Dietary Supplement 60-count caplets. The recalled dietary supplement is in a white box with "Women's Iron Complete" printed on the front in gray and red font. The box contains blister packets with a total of sixty caplets.

This recall involves all Pain Relief Naturally lidocaine-containing products including Numbify, Extra Strength Numbify, Pre-TAT Tattoo, Superior Pain & Itch Relief, and Soothing Sore Relief creams, sprays, gels and liquid gels. The recalled products were sold in 1, 2 and 4 ounce size containers. The products have black packaging with the name of the product in gold, red, or green lettering. Numbify Cream, Spray, Gel & Liquid Gel Black tubs and bottles with gold lettering Extra Strength Numbify Cream, Spray, Gel & Liquid Gel Black tubs and bottles with gold lettering Pre-TAT Tattoo Cream, Spray, Gel & Liquid Gel Black tubs and bottles with red lettering Superior Pain & Itch Relief Cream, Spray, Gel & Liquid Gel Black tubs and bottles with green lettering Soothing Sore Relief Cream, Spray, Gel & Liquid Gel Black tubs and bottles with green lettering

This recall involves UberScientific Uber Numb Topical Anesthetic Cream and Uber Numb Spray. The recalled cream is in a white jar with a smooth, rounded cap and a green label with "Uber Numb Topical Anesthetic Cream" printed on the front. The cream was sold in one, two and four ounce sizes with the lot numbers printed on the bottom of the jar and the UPC number printed on the label to the left of the product name. The brand name UberScientific is printed on the label below the net weight. The recalled spray is in a green bottle with a white cap and has a white label with "Uber Numb Spray" printed on the front. The spray was sold in four ounce size with the lot numbers printed on the bottom of the bottle and the UPC number printed on the label to the right of the product name. The brand name UberScientific is printed on the label to the left of the product name. Product Size UPC Lot Numbers UberScientific Uber Numb Topical Anesthetic Cream 1 oz. 00863255000306 A23Z3 and F12Z5 2 oz. 00863255000344 L06Z2A, L06Z2B, and B01N2A 4 oz. 0083255000313 E10Z4, L06Z2, and B01N2 Uber Numb Spray 4 oz. 00850777008002 K30Z6 and B09N2

The recalled Desert Harvest Reléveum Skin Repair Cream is in a transparent green bottle with a white pump dispenser cap and a tan/white gradient label with "Desert Harvest Reléveum" printed on the front. The product is an over the counter skin cream with lidocaine (4%) as the active ingredient. The cream is sold in a 4 ounce or an 8 ounce bottle with the date code "D02N5" printed above the barcode on the bottle.

This recall involves blister packages of prescription drugs from Novartis and Sandoz. The drugs are packaged with 3 to 10 tablets per blister card. The recalled Novartis prescription blister packages have "Novartis," the name of the drug, dosage, NDC, lot number and expiration date printed on the cartons and the blister cards. The recall includes the following: Recalled Novartis Prescription Drugs NDC Numbers Tablet Strength Carton Configuration Lot Numbers Expiration Date Zofran ODT® 0078-0679-61 0078-0679-19 4 mg 30 count: 3 cards with 10 tablets each 1657088 Dec 2019 Zofran ODT® 0078-0680-61 0078-0680-19 8 mg 30 count: 3 cards with 10 tablets each 1641546 Oct 2019 Entresto® (sacubitril/valsartan) 0078-0659-61 0078-0659-35 24 mg/ 26 mg 100 count: 10 cards with 10 tablets each FX000005 FX000004 FX000003 F0010 F0009 F0007 Apr 2020 Apr 2020 Sep 2019 Nov 2018 Aug 2018 Jul 2018 Entresto® (sacubitril/valsartan) 0078-0777-61 0078-0777-35 49 mg/ 51 mg 100 count: 10 cards with 10 tablets each FX000001 F0006 F0005 F0004 Dec 2019 Oct 2019 Aug 2019 Oct 2018 Entresto® (sacubitril/valsartan) 0078-0696-61 0078-0696-35 97 mg/ 103 mg 100 count: 10 cards with 10 tablets each FX000002 F0007 F0006 F0005 F0004 Mar 2020 Feb 2020 Dec 2019 Dec 2018 Oct 2018 The recalled Sandoz prescription blister packages have "Sandoz," the name of the drug, dosage, NDC and lot number printed on the cartons and the blister cards. Lot numbers are listed at www.us.sandoz.com/patients-customers/product-safety-notices. The recall includes the following: Recalled Sandoz Prescription Drugs Tablet Strength NDC Numbers Carton Configuration Azithromycin Tablets 250 mg 0781-5776-06 0781-5776-69 50 count: 5 cards with 10 tablets each Donepezil ODT Tablets 5 mg 0781-5276-06 0781-5276-64 30 count: 3 cards with 10 tablets each Donepezil ODT Tablets 10 mg 0781-5277-06 0781-5277-64 30 count: 3 cards with 10 tablets each Haloperidol Tablets 0.5 mg 0781-1391-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 1 mg 0781-1392-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 2 mg 0781-1393-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 5 mg 0781-1396-13 100 count: 10 cards with 10 tablets each Haloperidol Tablets 10 mg 0781-1397-13 100 count: 10 cards with 10 tablets each Imipramine HCl Tablets 25 mg 0781-1764-13 100 count: 10 cards with 10 tablets each Imipramine HCl Tablets 50 mg 0781-1766-13 100 count: 10 cards with 10 tablets each Isosorbide Dinitrate (ISDN) Tablets 10 mg 0781-1556-13 100 count: 10 cards with 10 tablets each Isosorbide Dinitrate (ISDN) Tablets 20 mg 0781-1695-13 100 count: 10 cards with 10 tablets each Naratriptan Tablets 2.5 mg 0781-5527-06 0781-5527-37 9 count: 1 card with 9 tablets Ondansetron Tablets 8 mg 0781-1681-33 3 count: 1 card with 3 tablets Ondansetron ODT 4 mg 0781-5238-06 0781-5238-64 30 count: 3 cards with 10 tablets each Ondansetron ODT 8 mg 0781-5239-06 0781-5239-64 30 count: 3 cards with 10 tablets each Ondansetron ODT 8 mg 0781-5239-06 0781-5239-80 10 count: 1 card with 10 tablets Perphenazine Tablets 2 mg 0781-1046-13 100 count: 10 cards with 10 tablets each Perphenazine Tablets 4 mg 0781-1047-13 100 count: 10 cards with 10 tablets each Perphenazine Tablets 8 mg 0781-1048-13 100 count: 10 cards with 10 tablets each Risperidone ODT 0.5 mg 0781-5310-06 0781-5310-08 28 count: 7 cards with 4 tablets each Risperidone ODT 1 mg 0781-5311-06 0781-5311-08 28 count: 7 cards with 4 tablets each Risperidone ODT 2 mg 0781-5312-06 0781-5312-08 28 count: 7 cards with 4 tablets each Risperidone ODT 3 mg 0781-5313-06 0781-5313-08 28 count: 7 cards with 4 tablets each Risperidone ODT 4 mg 0781-5314-06 0781-5314-08 28 count: 7 cards with 4 tablets each

The recalled Well at Walgreens Pain and Itch Relief Cream tube and packaging are orange with a purple stripe with "Maximum Strength," "Pain and Itch Relief Cream 4% Lidocaine" and "NET WT 2 OZ (56.7 grams)" printed in white on the front. The Well at Walgreens logo is located on the front upper right corner. The packaging contains the UPC bar code 3 11917 18962 8 on the back.

The recalled Synodrin Lidocaine Maximum Strength Pain Relieving Cream is in a white jar with a blue label with "Synodrin Lidocaine Maximum Strength 4% Pain Relieving Cream" printed on the front. The jars measure about three inches in diameter, are three inches tall and weigh about 4 ounces. They were sold in a blue box with yellow letters "Lidocaine" and white letters "Maximum Strength 4% Pain Relieving Cream." The brand name Synodrin is printed on the jar and the box. The box and jar have UPC code 8 64751 00032 6 printed on the right side.

This recall involves Nature's Truth Slow Release 45mg Iron Supplement bottles. The 60 count, coated tablets were sold in a green bottle with a green flip top cap. "Nature's Truth," "SLOW RELEASE IRON" and "45 mg" are printed on a yellow label on the bottle. Lot number 29672 and the January 2019 [EXP 01/2019] expiration date are printed on the right side of the bottle.

The recalled burn relief gel is packaged in a blue box with white letters "Burn Relief" and red letters "Burn Relief Gel". The brand name is Assured™. Inside the box is a blue and white tube labeled "Burn Relief Gel" and measuring approximately 5 inches long by 1 inch wide and weighs about 0.7 ounces (20 grams). The packaging contains the UPC bar code: 6 39277 09311 0.

This recall involves "Well at Walgreens" Multivitamin Women 50+ tablets. The white plastic bottles contain 200 multivitamin tablets. "Well at Walgreens Multivitamin Women 50+" is printed on the bottle's white and silver label. A yellow band at the top of the label states "Value Size." UPC number 3-11917-17262-0 and one of the following lot numbers 000001 (EXP 9/2016), 000002 (EXP 12/2016) or 000003 (EXP 11/2016) are printed on the back of the bottles on a white label.

This recall involves all 60-count bags of cherry flavor Soft Chews Iron with Vitamin C dietary supplements. The pink re-sealable bag has an image of cherries and a leaf on the front of the package. "Soft Chews Iron with Vitamin C," "Cherry flavor," "Bariatric Fusion," "60 Soft Chews" and "Dietary Supplement" are also on the front. Lot number 14191C2 is printed near the bottom of the back of the bags being recalled.

This recall involves CreaMiser refrigerated coffee creamer dispensers for commercial use with model numbers 200, 210 and 400, digital thermometers and certain serial numbers. The plastic dispensers were sold in the following colors: black granite, gray granite and sand. Models 200 and 210 have two creamer dispenser stations and model 400 has four creamer dispenser stations. Model, serial number and "CreaMiser Products Corporation" are printed on a white sticker or metal name plate on the back of the dispensers. Model numbers Serial numbers 200 CP200-02001 through CP200-05151 210 CP210-00001 through CP210-01925 400 CP400-02001 through CP400-05500

This recall involves Country Life Target-Mins 25 mg iron supplements bottles. The bottle is brown with a black top and has a white label with a yellow banner at the top and a green banner at the bottom. The words "IRON," "Country Life" and "90 tablets" are printed on the label. Bar code 015794024927 and Lot Number 13A866B are printed on the far left side of the front label.

This recall involves Triaminic® Syrups and Theraflu Warming Relief® Syrups for coughs, colds and fevers. There are 24 types of these two products included in the recall. A complete list of products, lot numbers and National Drug Codes (NDC) can be found at www.novartisOTC.com. Lot numbers are located on the bottom panel of the box and on the left side of the label on the bottle. The NDC number is located on the upper right corner of the front panel of the Triaminic Syrups box and the upper left corner of the Theraflu Warming Relief Syrups bottle.

The recalled supplement bottles are brown glass bottles that contain MegaFood One Daily Tablets. The bottles have a yellow label on the front with the words "MegaFood," "Fresh From Farm To Tablet," "One Daily," "Nourish," "Balance" and "Replenish" printed above a picture of vegetables. Recalled bottles have the following amounts, product codes and lot numbers: Amount Product Code Lot Numbers 60 tablets 51494 10151 10613, 10724 through 10728, 11246 and 12191 90 tablets 51494 10152 180 tablets 51494 10153 The amount is on the bottom right of the front label. The product code and lot numbers are on the left side of the front label.

The mounting systems were sold for use in hospital Intensive Care Units. The units are off-white and have multiple joints between the ceiling mount and the TV mount at the end of the arm system.

The dippers are metallic gray aluminum with a plastic dome-shaped cap on the base of the handle. "Pampered Chef" is imprinted in the cap. The ice cream dippers measure around seven inches in length. A non-toxic liquid is sealed inside the handle of the product which conducts the heat of your hand to more easily scoop hard ice cream.

The recalled supplements were sold in white plastic bottles. "Live Better Complete Multivitamin One Daily Maximum Formula" is printed in blue and red on a white label on one product and "Live Better Complex Vitamin B50" is printed in blue and green on a white label on the other product.

This recall only involves the following four products with the noted lot numbers: GNC Women's Ultra Mega 28-count multivitamin bottles with lot numbers 0432AL1781 and 1283CL1781, GNC Women's Ultra Mega Active 180-count multivitamin bottles with lot numbers 1029BL1783 and 1030BL1783, GNC Women's Ultra Mega Energy and Metabolism 90-count multivitamin bottles with lot number 1450CL1789 and GNC Prenatal Formula with Iron 120-count multivitamin bottles with lot number 0785BL2863. The lot numbers are printed on the side of the bottle and on the bottom of the product's packaging. The affected lots are packaged in a white plastic bottle with a white label and a flip-top cap.