Teligent Pharma recalls 0.05% Fluocinonide Topical Solution due to manufacturing quality issues. Products with NDC 52565-025-20 or 52565-025-59 are affected. No action needed as the firm is discontinuing 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% Fluocinonide Topical Solution in 20mL and 60mL bottles due to quality control issues. This recall happens because the company stopped its stability testing program, but there's no risk of injury to users.
The product was recalled because Teligent Pharma discontinued its stability testing program, which means the company can no longer confirm the product's safety over time. However, the recall does not indicate any immediate safety risk to users.
People who have the 20mL or 60mL bottles with NDC numbers 52565-025-20 or 52565-025-59. These products are prescription-only and not for general use.
Check for 20mL or 60mL bottles labeled with NDC 52565-025-20 or 52565-025-59. These are prescription-only products sold by Teligent Pharma in New Jersey.
Look for the NDC numbers 52565-025-20 or 52565-025-59 on the bottle label.
The recall is due to the company stopping stability testing, but there's no indication of immediate safety risks. The product is still safe for use as long as it's within its expiration date.
No action is required. The recall is for quality control reasons, not because the product is unsafe.
The official notice doesn't specify a disposal or return process. You can safely discard it if you want, but there's no requirement.
We’ve drafted a message you can send Teligent Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0685-2022 — Teligent Pharma Teligent Pharma Hello, I own a Teligent Pharma that is covered by recall D-0685-2022 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.
