CLASS II ONGOING Drug recall · Reported 11 Dec 2024 · FDA Enforcement Report

Genuine Joe Antibacterial Lotion Soap , Chloroxylenol recalled

Midlab is recalling Genuine Joe Antibacterial Lotion Soap , Chloroxylenol 0.1%, distributed nationwide in the US. The recall was initiated on 6 Nov 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot 0711241

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-0091-2025
FDA event ID
95826
Recalling firm
Midlab, Athens, TN
Classification
Class II
Status
Ongoing
Recall initiated
6 Nov 2024
FDA classified
2 Dec 2024
Reported
11 Dec 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

6 Nov 2024Recall initiated by company
2 Dec 2024Classified by FDA+26 days
11 Dec 2024Published in enforcement report+9 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: Out of specification results for micro in hand soap products.

Potency and specification recalls happen when a batch tests outside its approved limits for strength, purity or dissolution, which can mean the dose delivered is higher or lower than labelled.

Product as listed by the FDA

Genuine Joe Antibacterial Lotion Soap , Chloroxylenol 0.1%, 1 GALLON (3.78L), Manufactured in the U.S.A. for S.P. Richards Co., Atlanta, GA 30339

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Why was it recalled?

cGMP Deviations: Out of specification results for micro in hand soap products.

Which lots are affected?

Lot 0711241

Where was it sold?

Nationwide in the USA

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

Other products in this recall event

5 other products · FDA event 95826

This product is part of a recall event; the main page for the event is Royalab Germ Away Antibacterial Hand Soap recalled.

More recalls from Midlab

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