Teligent Pharma recalls 0.05% Halobetasol Propionate Ointment tubes 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 0.05% Halobetasol Propionate Ointment tubes because the manufacturer stopped its stability testing program. This means all products within their expiry dates are being recalled, even though they haven't been reported as unsafe.
The manufacturer discontinued its stability testing program, which means they can't confirm the product's safety over time. However, the recall is based on quality control deviations, not immediate safety risks.
Prescription users of the ointment who have the specific tube sizes and batch numbers listed in the recall. Patients using the product for skin conditions are most at risk.
Check for the ointment tube labeled 'Halobetasol Propionate Ointment, 0.05%, Net Wt. 50 grams' with the batch numbers 15720 (expiring 6/30/2022) or 16449/16450 (expiring 2/28/2023).
Look for the ointment tube with the specific batch numbers and expiration dates listed in the recall notice.
The recall is due to the manufacturer discontinuing stability testing, not immediate safety risks. The product is still safe for use until the expiration date.
No, the recall does not require stopping use. The product is safe until its expiration date, but all products within expiry are being recalled due to quality control issues.
Check the tube for the specific batch numbers: 15720 (expiring 6/30/2022) or 16449/16450 (expiring 2/28/2023).
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0691-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0691-2022 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.
