PROBLEND Hand Sanitizer recall — Class II (D-0360-2024) · pharmaranks
Class IITerminated
PROBLEND Hand Sanitizer recall
FDA recall D-0360-2024 · initiated Feb 19, 2024
May cause temporary or medically reversible harm; low probability of serious harm.
Why it was recalled
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Details
Product
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
Recalling company
Seatex LLC
Classification
Class II
Status
Terminated
Type
Voluntary: Firm initiated
Distribution
Nationwide in the US and Puerto Rico
Initiated
Feb 19, 2024
FDA report date
Mar 6, 2024
What to do.If you have a recalled product, don't throw away questions — check the FDA notice for the affected lot numbers and expiration dates, and ask your pharmacist or doctor before stopping a prescribed medicine. This page reproduces public FDA data and is not medical advice.