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Serious recall: Injury is possible or has been reported. Take action promptly.

Teligent Pharma, Inc. 2022-01-05 Health serious FDA
Health · FDA · Recall #FDA-D-0297-2022

Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, … Recall

Issued January 5, 2022 · Teligent Pharma, Inc.

In January 2022, Teligent Pharma, Inc. recalled the Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, …, a serious health recall reported by the FDA. Affected owners are eligible for a voluntary. Here is what the hazard is and exactly what to do about it.

Compiled by Maya Ellison, RecallCheckr

What this means for you

Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing

What you should do

  1. 1 Stop using Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle, (29 g), Rx Only, … right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact Teligent Pharma, Inc. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
Teligent Pharma, Inc.
Category
Health
Recall date
January 5, 2022
Units affected
Not reported
Sold at
Distributed Nationwide in the USA
Recall number
FDA-D-0297-2022
Made in
United States
Issuing agency
FDA

In context

  • Teligent Pharma, Inc. has 17 recalls in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 870th Health recall we've logged in 2022.
Read the official FDA notice

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