Scynexis recalls specific lot numbers of BREXAFEMME (Ibrexafungerp) 150mg tablets for potential cross-contamination with ezetimibe. This may affect patients using these medications.
Cross Contamination with Other Products: Potential cross-contamination of ibrexafungerp citrate drug substance with ezetimibe (a non-antibacterial beta-lactam compound).
Scynexis has recalled certain lots of BREXAFEMME (Ibrexafungerp) 150mg tablets due to a risk of cross-contamination with ezetimibe. This could affect patients taking the medication, though the risk is not described as causing serious injury.
The medication may have been contaminated with ezetimibe, a non-antibacterial beta-lactam compound. This cross-contamination could potentially affect the drug's safety and effectiveness for patients.
Patients prescribed BREXAFEMME (Ibrexafungerp) 150mg tablets by a doctor. Those most at risk are individuals taking the medication who may have been exposed to the recalled lots.
Check if you have BREXAFEMME (Ibrexafungerp) 150mg tablets in 4-count cartons with NDC 75788-115-04. Look for lot numbers LF21000008 (expiring 11/30/2023) or LF22000051 (expiring 11/30/2025).
Identify if your medication has NDC 75788-115-04 and lot numbers LF21000008 or LF22000051.
The recall is for potential cross-contamination with ezetimibe, but the record does not specify any risk of serious injury or harm.
The recall record does not provide a specific remedy, so you should contact your doctor or pharmacist for guidance.
Check the NDC number (75788-115-04) and lot numbers (LF21000008 or LF22000051) on your medication label.
We’ve drafted a message you can send Scynexis to request your refund or repair — edit it as you like.
Subject: Recall D-0042-2024 — Scynexis Scynexis Hello, I own a Scynexis that is covered by recall D-0042-2024 from Scynexis. 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.
