Kroger Arthritis Pain Acetaminophen, 225 count bottles
Summary
CPSC recalled Kroger Arthritis Pain Acetaminophen, 225 count bottles by Aurobindo Pharma Limited, of Telangana, India. 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.. Remedy: 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..
Details
Source
cpsc
External ID
22164
Action Date
2022-06-16
Status
Ongoing
Category
product
Product Description
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.
Context & Analysis
Aurobindo Pharma Limited, of Telangana, India has 4 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
How often does Aurobindo Pharma Limited, of Telangana, India have FDA actions?
Aurobindo Pharma Limited, of Telangana, India has 4 FDA actions in our database, including 2 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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