PROBLEND E3 Foaming Hand Sanitizer — Class II drug recall D-0357-2024
Terminated recall by Seatex LLC, reported 2024-03-06, distributed nationwide. CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
| Recall number | D-0357-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Seatex LLC, Rosenberg, TX, United States |
| Recall initiated | 2024-02-19 |
| Classified | 2024-02-29 |
| Reported by FDA | 2024-03-06 |
| Terminated | 2025-08-15 |
| Distributed | Nationwide (US) |
| Quantity | 274 cases |
| Reason classes | cgmp |
| Lot numbers | 265029, 273759 |
| Expiration dates | 2024-03-27, 2024-11-29 |
Product
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
Reason for recall
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-0357-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.