Akron Pharma, Inc. recalls Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC…
Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
Read the official notice →- Date
- 2022-08-24
- Country
- United States
- Brand
- Akron Pharma
- Product
- Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (NDC…
- Classification
- Class III
- Units
- Product was distributed to 6 distributors/wholesalers who may have further…
- Category
- Drugs & medical
- Source
- FDA · Drug
Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer
What to do
- Check the product name, strength and lot number against the official notice.
- Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
- Ask the pharmacy or supplier about a replacement or refund.
General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.
More Akron Pharma recalls
- 2025-01-22
USAkron Pharma, Inc. recalls Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC…
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
- 2024-10-30
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- 2023-03-15
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Akron Pharma, Inc. recalls DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-2829-1
Labeling: Incorrect or Missing Lot and/or Exp Date
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