Reported Jan 22, 2025 · Ongoing
Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US…
Akron Pharma, Inc.
Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Akron Pharma, Inc. · 373 Us Highway 46 Ste 117 · Fairfield, NJ · 07004-2456
Is this the product you have?
Acetaminophen Extra Strength 500 mg1000 Tablets per bottleAkron Pharma
- Manufactured for
Akron Pharma Inc373 US RT 46 W Building ESuite 117FairfieldNJ 07034NDC 71399-8022-02
- Lot codes and dates
Lot #s: KDT0224001BExp 08/31/2026KDT0224002BExp 09/30/2026
- Amount recalled
- 1232 bottles
This recall covers 7 products
The agency filed one notice per product. You are reading one of them; the other 6 are below.
Where it was sold
- Nationwide
Why it was recalled
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
This product is unlikely to cause harm, but it breaks a safety or labelling rule.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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