Seatex LLC: Drug Recall

Recall #D-0360-2024 · 02/19/2024

Class II: Risk

Recall Details

Recall Number: D-0360-2024
Classification: Class II
Product Type: Drug
Recalling Firm: Seatex LLC
Status: Terminated
Date Initiated: 02/19/2024
Location: Rosenberg, TX, United States
Voluntary/Mandated: Voluntary: Firm initiated
Product Quantity: 480 cases

Reason for Recall

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.

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

Distribution Pattern

Nationwide in the US and Puerto Rico

Other Recalls by Seatex LLC

Class II: Risk 02/19/2024

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class II: Risk 02/19/2024

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class II: Risk 02/19/2024

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class II: Risk 02/19/2024

CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class II: Risk 04/19/2023

Superpotent Drug and Failed Impurities/Degradation Products: formula does not adhere to the labeled specifications

View all recalls by Seatex LLC →

Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.