CLASS II Drug recall · Reported 20 Jun 2018 · FDA Enforcement Report

Acne Shave Post-Shave Moisturizer (salicylic acid), 5% tube recalled

Shadow Holdings is recalling Acne Shave Post-Shave Moisturizer (salicylic acid), 5% tube, distributed nationwide in the US. The recall was initiated on 25 May 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll lots
Quantity recalled15,216 tubes

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-0859-2018
FDA event ID
80184
Recalling firm
Shadow Holdings, Santa Clarita, CA
Classification
Class II
Status
Terminated
Recall initiated
25 May 2018
FDA classified
12 Jun 2018
Reported
20 Jun 2018
Type
Voluntary: Firm initiated
Customers notified by
Press Release

Timeline

25 May 2018Recall initiated by company
12 Jun 2018Classified by FDA+18 days
20 Jun 2018Published in enforcement report+8 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: products may be contaminated with bacteria.

Product as listed by the FDA

Acne Shave Post-Shave Moisturizer (salicylic acid), 0.5%, 3.3 FL OZ (98 mL) tube, Distributed by: United Exchange Corp., 17211 Valley View Blvd., Cerritos, CA 90703 USA, UPC 7 80707 73112 3.

Where it was distributed

Nationwide in the USA

Nationwide

Questions about this recall

Is Acne Shave Post-Shave Moisturizer (salicylic acid), 5% tube recalled?

Yes. Shadow Holdings recalled Acne Shave Post-Shave Moisturizer (salicylic acid), 5% tube on 25 May 2018. The recall is Class II and its status is Terminated. Recall number D-0859-2018.

Why was it recalled?

CGMP Deviations: products may be contaminated with bacteria.

Which lots are affected?

All lots

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 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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