Teligent Pharma recalls 0.1% Triamcinolone Acetonide Ointment USP 80g cartons due to incorrect labeling. This Rx-only product may be mispackaged and should be checked for proper labeling.
Correct Labeled Product Mispack
Teligent Pharma is recalling 0.1% Triamcinolone Acetonide Ointment USP 80g cartons because they were mispackaged. This recall affects prescription-only products that may have incorrect labeling, which could lead to improper use.
The product was mispackaged, meaning the labeling might not match the actual contents. This could lead to incorrect usage if the patient uses the wrong medication. However, the recall is for labeling issues, not safety risks.
Prescription patients who have received this specific ointment product. Those with medical conditions requiring this medication are most at risk if mislabeled.
Check for the product name 'Triamcinolone Acetonide Ointment USP 0.1% 80g', manufacturer 'Teligent Pharma', and lot number 16630 with expiration 03/2023.
Verify the product label matches the correct information: Triamcinolone Acetonide Ointment USP 0.1% 80g, Teligent Pharma, Lot #16630, Exp 03/2023.
The recall is for mispackaging, not safety risks. The product is safe if labeled correctly, but you should check the label to ensure it matches the specified details.
Look for the product name 'Triamcinolone Acetonide Ointment USP 0.1% 80g', manufacturer 'Teligent Pharma', and lot number 16630 with expiration 03/2023.
No, but you should check the label to ensure it matches the correct details before using. If it doesn't match, contact your healthcare provider.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0752-2021 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0752-2021 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.
