US Drug Recall Register
Class II · Moderate risk Ongoing Initiated Aug 14, 2023 (3 years ago)

All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Potential exposure to rodents and rodent activity in the distribution center. Also, due to unusually hot weather, FDA Recalled Products may have been subjected to temperatures in excess of storage condition instructions on product labeling.

What was recalled

All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.

Recalling firm
Inmar Supply Chain Solutions, LLC
Origin
TX, United States
Initiated by
N/A
FDA recall number
D-1104-2023

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.