# FDA recall D-0357-2024

> **Seatex LLC** · Class II · drug recall initiated 2024-02-19.

## 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.

## Distribution

Nationwide in the US and Puerto Rico

## Key facts

- **Recall number:** D-0357-2024
- **Recalling firm:** Seatex LLC
- **Classification:** Class II
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2024-02-19
- **Report date:** 2024-03-06
- **Termination date:** 2025-08-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rosenberg, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-0357-2024

## Citation

> AI Analytics. FDA recall D-0357-2024. Retrieved 2026-05-28 from https://api.ai-analytics.org/recall/D-0357-2024. Source: US FDA. Licensed CC0.

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