FDA Drug recall D-0357-2024
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
- FDA Drug
- Class II
- terminated
- Published 2024-03-06
On 2024-03-06 the FDA classified a Class II recall of PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471 by Seatex, citing CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0357-2024 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2024-02-19 |
| Published | 2024-03-06 |
| Last updated | 2026-09-13 11:52 UTC |
| Company | Seatex |
| Distribution | US |
Product
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
Reason
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Identifiers
| code_info | Lot #: 265029, Exp. 03/27/2024; 273759, Exp. 11/29/2024. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0357-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.