Reported Mar 30, 2022 · Terminated

Triamcinolone Acetonide Ointment USP, 0.1%, packaged in a) 15 grams tubes, NDC 52565-014-15; b) 80 grams tubes, NDC…

Teligent Pharma, Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Teligent Pharma, Inc. · 105 Lincoln Avenue · Buena, NJ · 08310

Is this the product you have?

4 of 4 products

Products covered by this recall
#Product as published
115 grams tubes, NDC 52565-014-15
280 grams tubes, NDC 52565-014-80
31 lb (454
4jars, NDC 52565-014-26; Rx only, Teligent Pharma, Inc., Buena, New Jersey 08310.
Lot codes and dates
  • Batch

    61 of 61 codes

    • a) 15000
    • Exp. 1/31/2023
    • 15591
    • Exp. 4/30/2023
    • 15946
    • Exp. 9/30/2023
    • b) 14674
    • Exp. 11/30/2022
    • 14760
    • 14798
    • Exp. 12/31/2022
    • 14896
    • Exp. 1/31/2023
    • 15000
    • Exp. 1/31/2023
    • 15591
    • Exp. 4/30/2023
    • 15802
    • 15833
    • Exp. 7/31/2023
    • 15872
    • Exp. 8/31/2023
    • 15946
    • Exp. 9/30/2023
    • 16069
    • Exp. 10/31/2023
    • 16199
    • Exp. 11/30/2023
    • 16429
    • Exp. 2/29/2024
    • 16608
    • 16712
    • Exp. 3/31/2024
    • 17080
    • Exp. 7/31/2024
    • c)15065
    • Exp. 2/28/2023
    • 15072
    • Exp. 2/28/2023
    • 15436
    • Exp. 3/31/2023
    • 15810
    • Exp. 7/31/2023
    • 15877
    • Exp. 8/31/2023
    • 15974
    • Exp. 9/30/2023
    • 16045
    • Exp. 10/31/2023
    • 16269
    • Exp. 12/31/2023
    • 16270
    • Exp. 12/31/2023
    • 16566
    • Exp. 3/31/2024
    • 16713
    • Exp. 3/31/2024
    • 17042
    • Exp. 6/30/2024
    • 17068
Amount recalled
482,003 tubes; 45,583 jars

This recall covers 37 products

The agency filed one notice per product. You are reading one of them; the other 36 are below.

24 more are in the archive.

Where it was sold

  • Nationwide
  • PR

Why it was recalled

cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Notice updated Jun 17, 2024 · Data as of Sep 19, 7:59 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.