Time-Cap Labs is recalling about 209,430 bottles of Kroger brand Aspirin (81 mg) and Ibuprofen (200 mg) because the packaging is not child-resistant as required by the Poison Prevention Packaging Act. The recall includes 300-count bottles of green and yellow labeled Low Dose Aspirin and 160-count bottles of blue and white labeled Ibuprofen softgel capsules. No incidents or injuries have been reported to date. Consumers should immediately move these products to a safe location out of reach and sight of children and contact Kroger for a full refund.
The bottle caps on these products are not child-resistant, posing a serious risk of poisoning if a young child accesses and swallows the contents. Aspirin and ibuprofen are regulated substances that must be in protective packaging to prevent accidental ingestion by children.
Consumers should immediately store the recalled products 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.
Label states Kroger, Low Dose, Aspirin, 81 mg Delayed-Release Tablets / Pain Reliever.
Label states Kroger, Ibuprofen, Capsules, 200 mg Pain Reliever / Fever Reducer.
Recalled Kroger Aspirin, 81 mg Delayed-Release enteric coated tablets, 300 count bottle
Recalled Kroger Ibuprofen, 200 mg softgel capsules, 160 count bottle
If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.
This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.
AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.
Sources: CPSC Notice · Raw API Response