Teligent Pharma recalls specific batches of Triamcinolone Acetonide Lotion USP 0.025% 60mL bottles due to discontinued stability testing. All recalled products are no longer available for prescription use.
cGMP deviations: all products within expiry are being recalled because the firm is discontinuing its stability study program.
Teligent Pharma is recalling certain batches of Triamcinolone Acetonide Lotion USP 0.025% 60mL bottles because the company stopped its stability testing program. This means the product may not be safe for long-term use as the quality control process was discontinued.
The recall is due to Teligent Pharma discontinuing its stability testing program, which means the product's quality and safety over time could be compromised. This affects the product's ability to maintain effectiveness and safety for the intended medical use.
Prescription patients who have the specific batch numbers listed in the recall notice. Patients using the product for medical purposes are most at risk due to potential quality issues.
Check the product label for the specific batch numbers listed: 14796 (expiring 12/31/2022), 14797 (expiring 1/31/2023), and other batches with expiration dates through 5/31/2024. The product is a prescription-only 60mL lotion.
Look for the batch numbers listed in the recall notice on the product label.
Teligent Pharma is recalling these products because they discontinued their stability testing program, which could affect the product's long-term safety and effectiveness.
No, only specific batch numbers with expiration dates through 5/31/2024 are affected as listed in the recall notice.
Check the product label for the batch numbers listed in the recall notice. If you have the affected batch, contact your healthcare provider for guidance.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0698-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0698-2022 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.
