Recalls: Nonglass Bottles or Jars

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. Read more.

This recall involves "The Best Damn Liquids" branded liquid nicotine products in all flavors packaged in clear plastic bottles in 120 mL and 240 mL sizes with a continuously threaded closure. Read more.

This recall involves Pro Supply Outlet sodium and potassium hydroxide products sold in two-pound rigid white plastic jars with continuous thread caps. The front of the label bears the PSO logo, the product name, SKU 7023 and UPC 078345004533 for the sodium hydroxide and SKU 7132 and UPC 078345004625 for the potassium hydroxide. Read more.

This recall involves bottles of the prescription drug Evrysdi, a prescription medicine used to treat spinal muscular atrophy (SMA) in adults and children 2 months of age and older. The recalled 100 mL amber bottles have "Evrysdi (risdiplam) for oral solution," the dosage and "NDC 20242-175-07" on the front of the bottle labels. Read more.

This recall involves fourteen different models of pre-diluted or concentrated antifreeze sold under six different brand names: Prestone®, AutoZone®, Highline®/Prime Guard®, Supertech®, Prime® and Starfire®. The one-gallon antifreeze bottles are black, gray, orange, white or yellow. The brand is printed on the front of the antifreeze. The date code and model numbers can be found on the back informational panel of the product. Only antifreeze products with the following brand name, model number and date codes are included on this recall: Product Name Model Number Date Codes PRESTONE 50/50 Antifreeze AF2100/G2F OF20118 OF20128 OF20129 OF20132 OF20133 OF20134 OF20135 OF20141 PRESTONE Concentrate Antifreeze AF2000/G2F OF20128 OF20134 OF20135 OF20141 PRESTONE COMMAND® Nitrite Free 50/50 AFC12100/F OF20062 PRESTONE Heavy Duty Antifreeze 50/50 AF5200/F OF20062 OF20063 PRESTONE AMM 33% Export Antifreeze AF2033 OF20111 AUTOZONE AMAM 50/50 Antifreeze 540721/1F OF20036 OF20037 OF20038 OF20041 OF20050 OF20055 OF20056 OF20085 OF20086 OF20094 OF20113 OF20133 OF20134 OF20135 AUTOZONE Concentrate 50/50 Antifreeze 000367/1F OF20041 OF20042 OF20056 OF20057 OF20062 OF20135 OF20139 HIGHLINE AMAM "Prime Guard" 50/50 Antifreeze HLAMAM5050GL/F OF20007 OF20008 OF20042 OF20043 OF20050 HIGHLINE AMAM "Prime Guard" Concentrate Antifreeze HLAMAMGL/F OF20042 SUPERTECH Antifreeze Pre Diluted ST4053/F OF20006 OF20007 OF20051 OF20055 OF20084 OF20070 OF20085 SUPERTECH Antifreeze ST4003/F OF20141 PRIME Antifreeze AMAM AF3000/F OF20049 OF20078 OF20140 PRIME AMAM 50/50 Antifreeze AF3100/F OF20043 OF20044 OF20078 OF20079 OF20140 STARFIRE Antifreeze AMAM 50/50 CPAMAM5050/F OF20057 Read more.

The recall involves 31 different over-the-counter drugs purchased on or after June 1, 2018 that are unexpired from the following brands: Medi-First, Medi-First Plus, Medique, Dover, Otis Clapp, and Ecolab. They include aspirin-containing products, acetaminophen-containing products, ibuprofen-containing products, lidocaine-containing products, diphenhydramine, loperamide, and naproxen products. The expiration date for tablets and creams can be found on either the top or side panels of the container carton in the format [YEAR/MO]. For products in spray bottles, the expiration date in the same format is located on the front of the bottle. The expiration date is found on the bottom for the spray cans. The 31 different recalled products are listed in the table below: Product Drug Package Type # of Packets Medi-First Non-Aspirin Acetaminophen acetaminophen (325 mg) 2 tablets packet 50 250 Medi-First Extra Strength Non-Aspirin Acetaminophen acetaminophen (500 mg) 2 tablets packet 50 125 250 Medi-First Sinus Pain & Pressure acetaminophen (500 mg) 2 tablets packet 50 125 250 Medique APAP acetaminophen (325 mg) 2 tablets packet 250 Medique Extra Strength APAP acetaminophen (500 mg) 2 tablets packet 50 125 250 Medique Back Pain-Off acetaminophen (250 mg) 2 tablets packet 50 100 250 Medique CCP Caffeine Fee acetaminophen (325 mg) 2 tablets packet 50 250 Medi-First Cold Relief acetaminophen (325 mg) 2 tablets packet 50 125 250 Medique Cramp Tabs acetaminophen (325 mg) 2 tablets packet 50 125 250 Medique Decorel Forte Plus acetaminophen (325 mg) 2 tablets packet 50 250 Medique Medicidin-D acetaminophen (325 mg) 2 tablets packet 50 100 250 Dover Aminofen acetaminophen (325 mg) 2 tablets packet 250 Otis Clapp Back Quell acetaminophen (200 mg) 2 tablets packet 150 Otis Clapp Mygrex acetaminophen (500 mg) 2 tablets packet 150 Otis Clapp Valihist acetaminophen (325 mg) 2 tablets packet 150 Medi-First Pain Relief Extra Strength acetaminophen (110 mg) aspirin (162 mg) 2 tablets packet 50 100 250 Medi-First Plus Pain Zappers acetaminophen (250 mg) aspirin (250 mg) 2 tablets packet 50 125 Medique Pain-Off acetaminophen (250 mg) aspirin (250 mg) 2 tablets packet 50 100 250 Medi-First Aspirin aspirin (325 mg) 2 tablets packet 50 125 250 Medi-First Plus Aspirin aspirin (325 mg) 2 tablets packet 50 125 Medique Aspirin aspirin (325 mg) 2 tablets packet 12 100 250 Medique Diphen diphenhydramine (25 mg) 1 tablet packet 24 200 Medi-First Ibuprofen ibuprofen (200 mg) 2 tablets packet 4 50 125 250 Medique I-Prin ibuprofen (200 mg) 2 tablets packet 3 100 250 Dover Addaprin ibuprofen (200 mg) 2 tablets packet 250 Medi-First Burn Cream with Lidocaine lidocaine (0.9 grams) packets 25 Medi-First Burn Spray lidocaine HCl (2%) 2 oz bottle -- Medi-First Blood Clotting Spray lidocaine (4%) 3 oz bottle -- Ecolab Burn Cream lidocaine (0.9 grams) packets 25 Medique Diamode loperamide HCl (2 mg) 1 tablet packet 6 50 100 Medique Mediproxen naproxen sodium (220 mg) 1 tablet packet 50 100 Read more.

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. Read more.

This recall involves 4.4 fl. oz. (144 mL) and 8 fl. oz. (240 mL) plastic amber bottles with white flip top lids. The white oval label on the bottle displays the Dr. Adorable logo, product name and the volume amount of the bottle. Read more.

This recall involves six brands of sodium and potassium hydroxide products sold in two pound clear plastic bottles with a continuous thread closure cap. The products are commonly advertised as being used for home soapmaking projects and clearing drains. The lot numbers included in the recall are from 4001 to 9288 and are located on the bottom of the jar and on the side of the box. The brands of products and description of the packaging included in the recall are: Brand Description Distributed By Soap Supply Co. Lye yellow label BigTProducts Soap Makers Lye green label BigTProducts California Soap Supply dark blue label NG Inc. Combo Pure Solutions light blue label NG Inc. Red Crown High Test Lye red label Boyer Corporation Boyer Potassium Hydroxide Flakes white label Boyer Corporation Read more.

This recall involves blister packages of prescription medications Sandimmune® (cyclosporine capsules, USP) 100 mg soft gelatin capsules and Neoral® (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules from Novartis. Packages of Sandimmune 100 mg contain three blister cards with ten soft gelatin capsules per card and packages of Neoral 100 mg contain five blister cards with six soft gelatin capsules per card. The recalled blister packages have "Novartis," the name of the medication, dosage, NDC, lot number and expiration date on the outer package and on the blister cards. Only 100 mg doses of these medications with the following NDC and lot numbers and expiration dates are included in this recall: Recalled Prescription Drugs NDC Numbers Lot Numbers Expiration Date Sandimmune® (cyclosporine capsules, USP) 100 mg soft gelatin capsules 0078-0241-15 0078-0241-61 APCA136 APCA339 APCA793 APCC238 09/2020 02/2021 01/2022 07/2022 Neoral® (cyclosporine capsules, USP) MODIFIED 100 mg soft gelatin capsules 0078-0248-15 0078-0248-61 APCA437 APCA979 07/2020 03/2021 Read more.