Aurohealth Recalls Kroger Brand Acetaminophen Due to Failure to Meet Child Resistant Packaging Requirement; Risk of Poisoning
IngestionLead / chemical
The hazard
The recalled over-the-counter product contains the regulated substance acetaminophen which must be in child resistant packaging as required by the Poison Prevention Packaging Act (PPPA). The packaging of the products is not child resistant, posing a risk of poisoning if the contents are swallowed by young children.
Incidents reported: None reported
What to do now
Consumers should immediately store the recalled product in a safe location out of reach and sight of children. Contact Kroger for information on how to properly dispose of the product and receive a full refund.
Contact: Kroger at 800-576-4377 (800-KRO-GERS) from 7 a.m. to 12 a.m. (midnight) ET Monday through Friday, 7 a.m. to 9:30 p.m. ET Saturday and Sunday, online atwww.kroger.com/i/recall-alerts, www.kroger.com and click on "Recall Alerts" at the bottom of the page, or www.aurohealth.com and click on "RECALL" at the top of the page for more information.
About this recall
This recall involves the Kroger brand acetaminophen. The red, white, and yellow label states, Kroger, Acetaminophen, Arthritis Pain, Extended-Release, Tablets USP, 650 mg, 225 extended-release tablets. The bottle has a red continuous thread gear closure. UPC number 041260012846 and lot numbers P2100890, P2100891, P2100992 (each with expiration date Aug-2023) and P2101010 (with expiration date Apr-2023) are included in this recall. The UPC number, lot number and expiration date are printed near the drug facts panel on the label on the back of the bottle.
Product photos
Photos: U.S. CPSC