Teligent Pharma recalls 0.05% Clobetasol Propionate 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 all 0.05% Clobetasol Propionate Ointment products because the company stopped its stability testing program. This affects all sizes (15g, 30g, 45g, 60g) with specific expiration dates and NDC numbers.
The recall is due to the company discontinuing its stability testing program, which means the product's quality and safety over time could be compromised. However, the product is still safe for use within its expiration date.
People who have the recalled ointment, which is prescription-only. Those using it for skin conditions are most at risk if they have ongoing medical needs.
Check for the ointment's NDC numbers: 52565-039-15 (15g), 52565-039-30 (30g), 52565-039-45 (45g), or 52565-039-60 (60g). It's a prescription-only product with specific expiration dates.
Identify the NDC number and expiration date on the ointment packaging to confirm if it's recalled.
The product is safe for use within its expiration date, but the recall is due to the company discontinuing stability testing, so it's being recalled for quality control reasons.
Check for NDC numbers 52565-039-15 (15g), 52565-039-30 (30g), 52565-039-45 (45g), or 52565-039-60 (60g) with specific expiration dates.
The recall does not require returning the product; it's a quality control issue that affects all products within their expiration dates.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0673-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0673-2022 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.
