RecallHawk

Kroger Aspirin, 300 count bottles and Ibuprofen, 160 count bottles

Unknown Manufacturer

Summary

CPSC recalled Kroger Aspirin, 300 count bottles and Ibuprofen, 160 count bottles by Unknown Manufacturer. Hazard: The recalled over-the-counter products contain the regulated substances aspirin and ibuprofen 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.. Remedy: 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..

Details

Source

cpsc

External ID

22160

Action Date

2022-06-16

Status

Ongoing

Category

product

Product Description

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

Context & Analysis

Unknown Manufacturer has 1320 FDA actions in our database.

Frequently Asked Questions

How often does Unknown Manufacturer have FDA actions?

Unknown Manufacturer has 1320 FDA actions in our database, including 0 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Use the link above to view the complete official filing. You can also use the openFDA API to query this record programmatically.

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