Teligent Pharma recalls 0.05% Desoximetasone 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% Desoximetasone Ointment products because the company stopped its stability testing program. This means the ointment may not be safe for use as it was not tested for long-term quality.
The ointment was not tested for long-term stability because Teligent Pharma discontinued its stability study program. This means the product might not be safe for extended use, but it does not pose an immediate risk of injury.
People who have the recalled ointment, which is prescription-only, are affected. Those using it for skin conditions are most at risk if they don't follow the recall.
Check for 100g tubes with NDC 52565-045-99 or 60g tubes with NDC 52565-045-60. The ointment is prescription-only and has specific expiration dates listed in the recall.
Look for the NDC codes 52565-045-99 (100g tubes) or 52565-045-60 (60g tubes) on the packaging.
The recall states that the ointment was not tested for long-term stability, but it does not indicate immediate safety risks. Teligent Pharma is discontinuing its stability testing program.
Check for 100g tubes with NDC 52565-045-99 or 60g tubes with NDC 52565-045-60. The ointment is prescription-only and has specific expiration dates listed in the recall.
The recall does not specify a remedy, so you should check with your healthcare provider or pharmacist for advice on safe use.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0677-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0677-2022 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.
