Recalling firm
Seatex LLC
Product type
Drug
Status
Terminated
Report date
2024-03-06
Distribution
Nationwide in the US and Puerto Rico
Firm state
TX
Product quantity
274 cases
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Risk Management & CAPAReason for recall
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Product description
PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471
Code / lot info
Lot #: 265029, Exp. 03/27/2024; 273759, Exp. 11/29/2024.
Other recalls SPEQ maps to Risk Management & CAPA
See all Risk Management & CAPA recalls →Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.