Akron Pharma Recalls
11 recalls on record · August 24, 2022 to January 22, 2025 · Drugs
Recalls by year
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23
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25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46,
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W B
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
January 22, 2025DrugsFDA
Akron Pharma, Inc. recalls Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 117, F
Hazard: Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
October 30, 2024DrugsFDA
Akron Pharma, Inc. recalls OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL OZ (473 mL) bottle, Akron Phar
Hazard: CGMP Deviations
March 15, 2023DrugsFDA
Akron Pharma, Inc. recalls DIBUCAINE 1% HEMORRHOIDAL OINTMENT, 1 oz. (28 gm), Manufactured for: Akron Pharma Inc. Fairfield NJ 07004, NDC 71399-282
Hazard: Labeling: Incorrect or Missing Lot and/or Exp Date
August 24, 2022DrugsFDA
Akron Pharma, Inc. recalls Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-8022-01), b) 1000-count bottle (
Hazard: Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.
August 24, 2022DrugsFDA
Akron Pharma, Inc. recalls Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 1000-count bottle (NDC 71399-8024
Hazard: Failed Tablet/Capsule Specifications: Imprint "AP 325" is missing from the tablet.