CLASS II ONGOING Drug recall · Reported 23 Jul 2025 · FDA Enforcement Report

Power Stick for her PH Balanced Roll-On Antiperspirant recalled

A.P. Deauville is recalling Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, distributed nationwide in the US. The recall was initiated on 10 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot # 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402
Quantity recalled21,265 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-0548-2025
FDA event ID
97211
Recalling firm
A.P. Deauville, Easton, PA
Classification
Class II
Status
Ongoing
Recall initiated
10 Jul 2025
FDA classified
31 Jul 2025
Reported
23 Jul 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter

Timeline

10 Jul 2025Recall initiated by company
23 Jul 2025Published in enforcement report+13 days
31 Jul 2025Classified by FDA+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

Product as listed by the FDA

Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent, 1.8 oz./53 mL, A.P Deauville, LLC, PA 18040, NDC# 42913-038-00, UPC Code 815195019313

Where it was distributed

U.S. Nationwide

Nationwide

Questions about this recall

Is Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent recalled?

Yes. A.P. Deauville recalled Power Stick for her PH Balanced Roll-On Antiperspirant Deodorant with Powder Fresh Scent on 10 Jul 2025. The recall is Class II and its status is Ongoing. Recall number D-0548-2025.

Why was it recalled?

CGMP Deviations

Which lots are affected?

Lot # 032026B011, 032226B031, 051626C241, 061526C882, 071226D371, 071226D381, 082526E341, 082826E402

Where was it sold?

U.S. 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 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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