Status
Ongoing
Drug Enforcement D-1104-2023
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.
Classification
Class II
Report Date
August 30, 2023
Termination Date
—
Product Information
- Product description
- All Over-The-Counter (OTC) drug products warehoused, salvaged, and sold by Inmar.
- Product quantity
- Unknown
- Reason for recall
- 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.
- Recall initiation reason
- —
- Initial firm notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Distribution pattern
- Separate Distribution List (salvage buyers) provided by Inmar and will be uploaded. Final customer distribution unknown.
Location & Firm
- Recalling firm
- Inmar Supply Chain Solutions, LLC
- Address
-
1131 W Bardin Rd Ste 131, N/A
United States - Voluntary / Mandated
- N/A
- Status date
- —
Codes & Dates
- Recall number
- D-1104-2023
- Event ID
- 92884
- Recall initiation date
- August 14, 2023
- Center classification date
- August 24, 2023
- Code info
- Miscellaneous
- More code info
- —