DrugJan 22, 2025
Akron Pharma Diphenhydramine HCl 25 mg, 1000 Capsules per bottle, Akron Pharma recall — FDA D-0198-2025
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class IIIFDA: OngoingAkron Pharma, Inc.
Recall history in this database
Classification mix: Class III: 3.
DrugJan 22, 2025
Akron Pharma Diphenhydramine HCl 25 mg, 100 capsules per bottle, Akron Pharma recall — FDA D-0197-2025
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class IIIFDA: OngoingAkron Pharma, Inc.
DrugJan 22, 2025
Akron Pharma Acetaminophen Extra Strength 500 mg, 1000 Tablets per bottle, Akron Pharma recall — FDA D-0196-2025
Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.
Class IIIFDA: OngoingAkron Pharma, Inc.
Understanding this recall history
This page summarizes recall records in which the official source identifies Akron Pharma, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.