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Class III: unlikely to cause harmTerminated

Teligent Desoximetasone Ointment Recall

Desoximetasone Ointment USP, 0

Teligent, Inc. · Buena, NJ

Risk level
Class III
Reported by FDA
May 24, 2017
Recall ID
D-0787-2017
Check your lot numberHow we source this data

Summary

Teligent recalled Desoximetasone Ointment starting Apr 7, 2017. The FDA classified it as Class III (unlikely to cause harm) and published enforcement report D-0787-2017 on May 24, 2017. Reason: Superpotent Drug. Status: Terminated.

Why it was recalled

Superpotent Drug

Product description

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

Lot numbers, UPCs & expiration codes

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

Where it was sold

TN

What to do if you have this product

  • Compare the lot number and expiration date on your package with the codes above.
  • Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
  • If you have symptoms you think are related, contact your doctor. In an emergency call 911.
  • Report side effects to FDA MedWatch at 1-800-FDA-1088.

Recall details

Recall number
D-0787-2017
Classification
Class III
Status
Terminated
Recall initiated
Apr 7, 2017
FDA report date
May 24, 2017
Quantity
3600 tubes
Recall type
Voluntary: Firm initiated
Recalling firm
Teligent, Inc.

Original FDA data

Every field from FDA enforcement report D-0787-2017, exactly as published.

Show all FDA fields
City
Buena
State
NJ
Status
Terminated
Country
United States
Event ID
77061
Address
105 Lincoln Avenue
Code information
Lot #: 5760, Exp. 5/31/2018
Postal code
08310
Report date
May 24, 2017
Product type
Drugs
Recall number
D-0787-2017
Classification
Class III
Recalling firm
Teligent, Inc.
Product quantity
3600 tubes
Termination date
Feb 20, 2018
Reason for recall
Superpotent Drug
Voluntary / mandated
Voluntary: Firm initiated
Product description
Desoximetasone Ointment USP, 0.25%, 15 g tubes, Rx Only, Teligent Pharma, Inc. Buena. New Jersey 08310 NDC 52565-030-15
Distribution pattern
TN
Recall initiation date
Apr 7, 2017
Initial firm notification
Letter
Center classification date
May 18, 2017

How we source this data

Source: U.S. Food and Drug Administration enforcement report D-0787-2017, published May 24, 2017. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

FindMyRecall is an independent service and is not affiliated with or endorsed by the FDA. This page simplifies the official record; the FDA or manufacturer notice is authoritative, so follow its instructions. Medication information here is not individualized medical advice.

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