Teligent Pharma recalls 0.5% Triamcinolone Acetonide Ointment due to quality control issues. All products within expiry are being recalled as the company discontinues stability testing.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Teligent Pharma is recalling 0.5% Triamcinolone Acetonide Ointment tubes because the company stopped its stability testing program. This affects prescription-only products with specific batch numbers and expiration dates.
The recall is due to the company discontinuing its stability testing program, which means the product's quality and safety over time could not be confirmed. This is a quality control issue, not a direct safety hazard like injury or contamination.
Prescription patients who have received this ointment from Teligent Pharma. Patients with the specific batch numbers and expiration dates listed are most at risk.
Check for the ointment tube labeled 'Triamcinolone Acetonide Ointment USP, 0.5%, Net Wt. 15 grams' with the manufacturer Teligent Pharma. Look for batch numbers 15608, 16026, or 16224 and expiration dates 5/31/2022, 9/30/2022, or 11/30/2022.
Identify the batch number and expiration date on the ointment tube to confirm if it is part of the recall.
The company discontinued its stability testing program, so the product's quality and safety over time could not be confirmed.
No, this is a quality control issue, not a direct safety hazard like injury or contamination.
Check the batch number and expiration date to see if it is part of the recall. If it is, contact Teligent Pharma for further instructions.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0696-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0696-2022 from Teligent Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
