Akron Pharma, Inc. recalls

8 recalls on record · latest: December 12, 2024

Official U.S. recall history for Akron Pharma, Inc., compiled from official government records.

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Akron Pharma, Inc. recalls Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., 373 US…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

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,…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Akron Pharma, Inc. recalls Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US 46 W Building E, Suite 11…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Akron Pharma, Inc. recalls Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc. 373 Route US 46…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Akron Pharma, Inc. recalls Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron Pharma, Inc., 373 RT US 46 W…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Akron Pharma, Inc. recalls Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ…

December 12, 2024 · Drug & medication recalls Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

OneLAX Docusate Sodium Liquid Stool Softener Laxative recalled over manufacturing violations

October 15, 2024 · Drug & medication recalls Moderate risk CGMP Deviations