FDA recall D-0195-2025

Akron Pharma, Inc. · Class III · drug

Product

Acetaminophen, 325 mg Tablets, 100 Tablets per bottle, Akron Pharma, Manufactured for: Akron Pharma Inc., Fairfield, NJ 07034, NDC 71399-8014-01.

Reason for recall

Labeling: Not Elsewhere Classified: Tablets/Capsules imprinted with wrong ID.

Distribution

Nationwide in the US

Key facts

Status
Ongoing
Initiation date
2024-12-12
Report date
2025-01-22
Voluntary/Mandated
Voluntary: Firm initiated
Location
Fairfield, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0195-2025