Central Admixture Pharmacy Services recalls sterile injectable medication due to potential contamination. Products may not be sterile, posing infection risks. Affected lots and expiration dates listed.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling Modified del Nido Microplegia injections because an FDA inspection found possible contamination. Using these products could lead to infections since they're meant to be sterile.
The products were found by the FDA to potentially lack sterility. This means the medication might contain harmful bacteria or other contaminants that could cause infections when injected.
Healthcare professionals and patients who use this medication under prescription. Those handling the product at pharmacies or clinics are most at risk.
Check for the lot numbers 37-893821 through 37-999585 and expiration dates listed in the recall notice. The product is a 40 mL per syringe injection prescribed only by a doctor.
Identify the lot number and expiration date on the syringe packaging to confirm if it's affected.
An FDA inspection found potential contamination, meaning the products might not be sterile and could cause infections if used.
Check the lot number and expiration date. If it matches the recalled lots, contact your pharmacy or healthcare provider for guidance.
The recall indicates a risk of contamination, so it's not safe to use until the affected lots are replaced.
We’ve drafted a message you can send Central Admixture Pharmacy Services to request your refund or repair — edit it as you like.
Subject: Recall D-0681-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0681-2023 from Central Admixture Pharmacy Services. 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.
