CLASS II Drug recall · Reported 6 Mar 2024 · FDA Enforcement Report

Problend Hand Sanitizer, Refreshing Gel Hand Sanitizer recalled

Seatex is recalling Problend Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic, distributed nationwide in the US. The recall was initiated on 19 Feb 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 266029, Exp. 03/27/2024.
Quantity recalled480 cases

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0360-2024
FDA event ID
93986
Recalling firm
Seatex, Rosenberg, TX
Classification
Class II
Status
Terminated
Recall initiated
19 Feb 2024
FDA classified
29 Feb 2024
Reported
6 Mar 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail

Timeline

19 Feb 2024Recall initiated by company
29 Feb 2024Classified by FDA+10 days
6 Mar 2024Published in enforcement report+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Product as listed by the FDA

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

Where it was distributed

Nationwide in the US and Puerto Rico

Nationwide Puerto Rico

Questions about this recall

Is Problend Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic recalled?

Yes. Seatex recalled Problend Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic on 19 Feb 2024. The recall is Class II and its status is Terminated. Recall number D-0360-2024.

Why was it recalled?

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

Which lots are affected?

Lot #: 266029, Exp. 03/27/2024.

Where was it sold?

Nationwide in the US and Puerto Rico

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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