Published recall report · Labelling errorUpdated · 1 yr 8 mo ago
Akron Pharma, Inc. recall: Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
Current recall status is unverified. FDA does not update drug-enforcement status after publication. Check the latest official information or ask a pharmacist.
What to do
Check the lot number on your pack against this recall and follow the firm's instructions. Do not stop taking a prescribed medicine without talking to a pharmacist or doctor first.
FDA public enforcement report, opens in a new tabWhich products
Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8022-01.
- Producer
- Akron Pharma, Inc.
KDT0224002A
- Dates on pack
- Lot: KDT0224002A, Exp 09/30/2026
More detail
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
In the news
Reporting from news publishers. Follow the official notice for product advice.
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