CLASS II ONGOING Drug recall · Reported 28 Aug 2024 · FDA Enforcement Report

Testosterone Gel, 1.62%, (Alcohol 80% v/v)-dose packets recalled

Teva Pharmaceuticals USA is recalling Testosterone Gel, 1.62%, (Alcohol 80% v/v)-dose packets, distributed nationwide in the US. The recall was initiated on 8 Aug 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot #: 100042386, Exp. Date 06/2025
NDC0591-2924, 0591-2925, 0591-2926
Quantity recalled7,080 unit dose packets

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-0637-2024
FDA event ID
95122
Recalling firm
Teva Pharmaceuticals USA, Parsippany, NJ
Manufacturer
Actavis Pharma, Inc.
Classification
Class II
Status
Ongoing
Recall initiated
8 Aug 2024
FDA classified
16 Aug 2024
Reported
28 Aug 2024
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

8 Aug 2024Recall initiated by company
16 Aug 2024Classified by FDA+8 days
28 Aug 2024Published in enforcement report+12 days

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

Reason for recall

Superpotent Drug

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

Testosterone Gel, 1.62%, (Alcohol 80% v/v), 30 unit-dose packets, Rx Only, Teva Pharmaceuticals, USA, Inc. North Wales, PA 19454, NDC 0591-2925-30. Packet NDC # 0591-2925-32 Carton NDC # 0591-2925-30

Where it was distributed

Product was distributed nationwide within the United States

Nationwide

Questions about this recall

Why was it recalled?

Superpotent Drug

Which lots are affected?

Lot #: 100042386, Exp. Date 06/2025

Where was it sold?

Product was distributed nationwide within the United States

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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