Central Admixture Pharmacy Services recalls fentanyl 2 mcg/mL and bupivacaine 0.0625% solutions in 0.9% sodium chloride due to lack of sterility assurance. This may cause infections if used improperly.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl and bupivacaine solutions that may not be sterile, posing infection risks. Healthcare providers using these products should stop using them immediately.
The solutions lack validation data for sanitization cycles, meaning they might not be sterile when prepared. This could lead to infections if used in medical procedures without proper sterility assurance.
Healthcare providers who use these specific fentanyl and bupivacaine solutions for medical procedures are affected. Patients receiving these treatments could face infections if the products are not properly sterile.
Check for the product name: fentanyl 2 mcg/mL and bupivacaine 0.0625% in 0.9% sodium chloride, 250 mL bags. Look for lot numbers 17-271814 through 17-272716 with expiration dates up to August 21, 2023.
Discontinue use of the recalled fentanyl and bupivacaine solutions as they may not be sterile.
The recalled product is fentanyl 2 mcg/mL and bupivacaine 0.0625% in 0.9% sodium chloride, 250 mL bags with specific lot numbers and expiration dates.
Check the lot number on the product label, which should be between 17-271814 and 17-272716, with expiration dates up to August 21, 2023.
The recall record does not specify any remedy; the product must be stopped and discarded immediately.
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-1069-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1069-2023 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.
