CLASS II Drug recall · Reported 1 Jul 2020 · FDA Enforcement Report

Soft Whisper by Powerstick Dandruff Shampoo recalled by A.P. Deauville

A.P. Deauville is recalling Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc), A.P. Deauville LLC New, distributed nationwide in the US. The recall was initiated on 3 Jun 2020 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 070421E211; 070921E221; 071021E231; 071021E241, Exp 7/2021
Quantity recalled82,800 bottles

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-1337-2020
FDA event ID
85806
Recalling firm
A.P. Deauville, New Brunswick, NJ
Classification
Class II
Status
Terminated
Recall initiated
3 Jun 2020
FDA classified
24 Jun 2020
Reported
1 Jul 2020
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

3 Jun 2020Recall initiated by company
24 Jun 2020Classified by FDA+21 days
1 Jul 2020Published in enforcement report+7 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: Soft Whisper Dandruff Shampoo was produced with water that failed USP specifications.

Product as listed by the FDA

Soft Whisper by Powerstick Dandruff Shampoo (Pyrithione Zinc), 14.4 FL OZ. (426 mL), A.P. Deauville LLC New Brunswick, NJ 08901, NDC 42913-020-00, UPC 815195014097

Where it was distributed

U.S.A. Nationwide

Nationwide

Questions about this recall

Why was it recalled?

cGMP Deviations: Soft Whisper Dandruff Shampoo was produced with water that failed USP specifications.

Which lots are affected?

Lot #: 070421E211; 070921E221; 071021E231; 071021E241, Exp 7/2021

Where was it sold?

U.S.A. Nationwide

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.

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