Central Admixture Pharmacy Services recalls fentanyl 2 mcg/mL and bupivacaine 0.0625% solution in 250mL due to lack of sterility assurance. This product is for medical use only and must be discarded if affected.
Lack of assurance of sterility:
Central Admixture Pharmacy Services has recalled a specific fentanyl and bupivacaine solution product due to a lack of sterility assurance. This means the product could cause infections if used improperly, and affected patients should not use it.
The product lacks proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. If used for medical injections, this could lead to serious infections in patients.
This recall affects patients who have been prescribed this specific fentanyl and bupivacaine solution by their healthcare provider. Medical professionals using this product for injections are most at risk of infection.
Check for the product name: fentanyl 2 mcg/mL and bupivacaine 0.0625% in 0.9% sodium chloride, 250 mL. The NDC code is 71286-2081-1, and the lot number is 17-275929 with an expiration date of 10/12/2023.
Verify the NDC code 71286-2081-1 and lot number 17-275929 on the product label.
No, this product has been recalled due to a lack of sterility assurance, which could cause infections if used.
The recall record does not specify a remedy, so contact your healthcare provider for guidance.
Check for the NDC code 71286-2081-1 and lot number 17-275929 on the product label.
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-0016-2024 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0016-2024 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.
