Published recall report · Labelling errorUpdated · 1 yr 8 mo ago
Akron Pharma, Inc. recall: Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .
Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .
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 Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, Fairfield, NJ 07004, NDC 71399-8024-01 .
- Producer
- Akron Pharma, Inc.
KDT0124001
- Dates on pack
- Lot #: KDT0124001, Exp 08/31/2026
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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