Biocon Pharma recalls 100mg Posaconazole Delayed-Release Tablets with high impurities. Affected lots expire Sep 2023-Dec 2023. Stop using if you have these specific batches.
Failed Impurities/Degradation Specifications: High Out Of Specification degradation results.
Biocon Pharma is recalling 100mg Posaconazole Delayed-Release Tablets due to high impurities that could cause harm. This recall affects specific batches with expiration dates through September 2023 and December 2023. The product is prescription-only and must be stopped if you have the affected lots.
The tablets contain high levels of impurities that may degrade the product quality. This degradation could potentially cause harm to patients taking the medication. The exact health risk is not clearly specified in the recall notice.
Prescription patients who have the specific batch numbers listed in the recall. Those with the affected lots (BF21003163, BF21003246, BF21003161, BF21004742, BF22003359) are most at risk.
Check the batch number on the product label. Affected batches include BF21003163, BF21003246, BF21003161, BF21004742, and BF22003359. The product expires by September 2023, December 2023, or September 2025.
Look for the batch number on the product label to determine if it is one of the affected lots.
The tablets contain high levels of impurities that may degrade the product quality, but the exact health risk is not clearly specified in the recall notice.
Affected batches include BF21003163, BF21003246, BF21003161, BF21004742, and BF22003359.
Check the batch number on the product label. The affected batches have specific numbers listed in the recall notice.
We’ve drafted a message you can send Biocon Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0268-2023 — Biocon Pharma Biocon Pharma Hello, I own a Biocon Pharma that is covered by recall D-0268-2023 from Biocon 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
