Akron Pharma, Inc. recalls Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US…
- Recall date
- December 12, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0196-2025
- FDA classification
- Class III
- Brand / firm
- Akron Pharma, Inc.
- Sold / distributed
- Nationwide in the US
Why it was recalled
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US RT 46 W Building E, Suite 117, Fairfield, NJ 07034, NDC 71399-8022-02
Get recall alerts
Free email alert whenever Akron Pharma, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Akron Pharma, Inc.