Recalls / Firms / Akron Pharma, Inc.

Akron Pharma, Inc.

11 FDA drug recalls on record.

Date	Class	Drug	Status
2024-12-12	Class III	Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma, Manufactured for: Akron	Ongoing
2024-12-12	Class III	Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akr	Ongoing
2024-12-12	Class III	Diphenhydramine HCl 50 mg, 1000 capsules per bottle, Akron Pharma, Manufactured for: Akron	Ongoing
2024-12-12	Class III	Acetaminophen Regular Strength, 325 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT	Ongoing
2024-12-12	Class III	Acetaminophen Extra Strength 500 mg, 100 Tablets per bottle, Akron Pharma, Inc., 373 RT US	Ongoing
2024-12-12	Class III	Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma, Manufactured for: Akron	Ongoing
2024-12-12	Class III	Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma, Manufactured f	Ongoing
2024-10-15	Class II	OneLAX Docusate Sodium Liquid (docusate sodium 50 mg/5 mL) Stool Softener Laxative, 16 FL	Ongoing
2023-02-17	Class III	Dibucaine	Terminated
2022-08-04	Class III	Acetaminophen 500 mg tablet, Extra Strength, packaged in a) 100-count bottle (NDC 71399-80	Terminated
2022-08-04	Class III	Acetaminophen 325 mg tablets, packaged in a) 100-count bottle (NDC 71399-8024-01); b) 100	Terminated