CLASS III Drug recall · Reported 24 May 2017 · FDA Enforcement Report

Desoximetasone Ointment USP, 25% tubes recalled by Teligent

Teligent is recalling Desoximetasone Ointment USP, 25% tubes, distributed in Tennessee. The recall was initiated on 7 Apr 2017 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesLot #: 5760, Exp. 5/31/2018
Quantity recalled3600 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-0787-2017
FDA event ID
77061
Recalling firm
Teligent, Buena, NJ
Classification
Class III
Status
Terminated
Recall initiated
7 Apr 2017
FDA classified
18 May 2017
Reported
24 May 2017
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Potency & Assay

Timeline

7 Apr 2017Recall initiated by company
18 May 2017Classified by FDA+41 days
24 May 2017Published in enforcement report+6 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

Desoximetasone Ointment USP, 0.25%, 15 g tubes, Rx Only, Teligent Pharma, Inc. Buena. New Jersey 08310 NDC 52565-030-15

Where it was distributed

TN

Tennessee

Questions about this recall

Is Desoximetasone Ointment USP, 25% tubes recalled?

Yes. Teligent recalled Desoximetasone Ointment USP, 25% tubes on 7 Apr 2017. The recall is Class III and its status is Terminated. Recall number D-0787-2017.

Why was it recalled?

Superpotent Drug

Which lots are affected?

Lot #: 5760, Exp. 5/31/2018

Where was it sold?

TN

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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