Central Admixture Pharmacy Services recalls fentanyl syringes with potential sterility issues. Lack of validation data for sanitization cycles poses a risk of contamination.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services has recalled specific fentanyl syringes due to a lack of validation data for sanitization cycles. This could lead to contamination risks if the syringes are used without proper sterility assurance.
The syringes were manufactured without sufficient validation data to ensure proper sanitization cycles. This lack of validation means there is a potential risk of contamination, which could lead to infections if the syringes are used without adequate sterility.
Healthcare professionals and patients prescribed fentanyl injections who received the recalled syringes. Those using the syringes for medical treatment are at risk of contamination.
Check for the product name 'fentaNYL in 0.9% sodium chloride, 10 mcg/1 mL, 3 mL Syringe' with the NDC code 71286-2071-1 and specific lot numbers listed in the recall notice.
Review the NDC code and lot numbers listed in the recall notice to confirm if your syringe is affected.
The recall indicates a potential sterility risk due to lack of validation data for sanitization cycles. Do not use the syringes until you confirm they are not recalled.
Check the NDC code and lot numbers listed in the recall notice to determine if your syringes are affected. If they are, contact the manufacturer for instructions.
Look for the NDC code 71286-2071-1 and specific lot numbers (17-270539 to 17-274044) listed in the recall notice.
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-1079-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1079-2023 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.
