Recalls: Plastic

This recall involves the Kroger brand acetaminophen over-the-counter drug. The red, white and gray label states Kroger, Acetaminophen, Extended-Release Tablets USP, 650mg, Pain Reliever/Fever Reducer, 100 caplets. The bottle has a white continuous thread closure. The UPC number is 041260012877 with the batch codes AC45463, AC38213 or AC30682. The location of the UPC number is under the bar code on the packaging and the batch code is at the bottom of the label on the bottle. Read more.

This recall involves the Walgreens brand acetaminophen product. The red and white label states Walgreens, Easy Open for Adults, Pain Reliever, Acetaminophen, 500 mg, Fever Reducer, Extra Strength, 150 caplets. The bottle has a red continuous thread gear closure. UPC number 311917218090 and Lot numbers P2100627, P2100671, P2100672, P2100689 P2100747, P2100859 (each with expiration date Nov-2022) and P2200050 (with expiration date Jan-2023) are included in this recall. The UPC number, lot numbers and expiration date are printed near the drug facts panel on the label on the back of the bottle. Read more.

This recall involves the Kroger brand aspirin and ibuprofen over-the-counter drugs. For the aspirin product, the green and yellow label states Kroger, Low Dose, Aspirin, 81 mg Delayed-Release Tablets / Pain Reliever, 300 enteric coated tablets. The bottle has a green continuous thread gear closure. For the ibuprofen product, the blue and white label states Kroger, Ibuprofen, Capsules, 200 mg Pain Reliever / Fever Reducer, 160 softgels. The bottle has a blue continuous thread gear closure. The following UPC and Lot numbers listed in the table are included in this recall and can be found on the label on the back of the bottle. Item UPC Lot numbers Aspirin 4126001295 A077J F032H F035H J011H K031H Ibuprofen 4126001298 FH1163 C11044 C11047 C11064 C11065 C11079 C11084 Read more.

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. 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 blister packages of prescription medications. The name and strength of the medication, "For Institutional Use only," "Rx Only," lot number and expiration date are printed on the outside of the package as well as on the individual blister units. The Dr. Reddy's logo and NDC number are printed on the outside of the package. The recalled medications include the following: Recalled Prescription Drugs NDC Numbers Carton Configurations Lot Numbers Expiration Dates Imatinib Mesylate Tablets 100 mg 43598-344-31 3 blister cards of 10 tablets H2000138 2022-0630 Imatinib Mesylate Tablets 400 mg 43598-345-31 3 blister cards of 10 tablets H2000127 2022-0630 Pregabalin Capsules 50 mg 43598-292-66 5 blister cards of 10 capsules T900876 2021-0630 Pregabalin Capsules 75 mg 43598-293-66 5 blister cards of 10 capsules T901021 2021-0731 Pregabalin Capsules 100 mg 43598-294-66 5 blister cards of 10 capsules T901022 2021-0731 Pregabalin Capsules 150 mg 43598-295-66 5 blister cards of 10 capsules T901023 2021-0731 Sevelamer Carbonate Tablets 800 mg 55111-789-11 4 blister cards of 25 tablets T801003, T000009, T900221 2020-1031, 2021-1231, 2021-0228 Tadalafil Tablets 5 mg 43598-575-31 3 blister cards of 10 tablets T000376 2022-0131 Tadalafil Tablets 20 mg 43598-573-31 3 blister cards of 10 tablets T000425 2022-0228 Read more.

This recall involves 50, 80, 100, 125, 200, 250 and 300-count bottles of Excedrin Migraine Caplets, Excedrin Migraine Geltabs, Excedrin Extra Strength Caplets, Excedrin PM Headache Caplets, and Excedrin Tension Headache Caplets. The bottles are plastic with a child-resistant closure. For a full list of the recalled products, visit www.excedrin.com/products/discontinued. 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.

This recall involves Sanvall Rapid Alivio Pain Relieving Roll-On in a 3 fl. oz (88.5 mL) white plastic bottle with a white cap and a red, white and blue label. "Rapid Alivio," "Maximum Strength Pain Relieving Liquid" and "Para Dolor Muscular" are printed on the label. Lot numbers 18032201, 18032301, 19040501, or 19052801 are printed on the bottom of the bottle. UPC code 605100014225 is printed on the side of the label. Read more.