D-0360-2024 Class II Terminated
FDA drug recall D-0360-2024 was initiated by Seatex LLC on February 19, 2024 and is designated Class II. Reason for recall: CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility. The recall status is terminated (terminated August 15, 2025). Affected quantity: 480 cases.
Recall Details
- Product Type
- Drugs
- Report Date
- March 6, 2024
- Initiation Date
- February 19, 2024
- Termination Date
- August 15, 2025
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 480 cases
Product Description
PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, mountain spring scent, 1250 mL cases, Seatex LLC, 445 TX Hwy 36 Rosenberg, YX 77471
Reason for Recall
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Distribution Pattern
Nationwide in the US and Puerto Rico
Code Information
Lot #: 266029, Exp. 03/27/2024.