Central Admixture Pharmacy Services recalls specific fentanyl syringes (NDC 71286-2071-3) due to lack of sterility assurance from sanitization cycles. Affected lots expire through September 2023.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling fentanyl syringes that may not be sterile due to insufficient validation of sanitization cycles. This could lead to infections if used improperly.
The syringes lack proper validation for sanitization cycles, meaning they might not be sterile. If used without proper sterilization, this could introduce infections into the patient's body.
Healthcare professionals using these syringes for medical treatments. Patients receiving fentanyl injections via these syringes are at risk of infection.
Check for the NDC number 71286-2071-3 on the syringe label. The affected lots include specific expiration dates from July 2023 through September 2023.
Look for the NDC number 71286-2071-3 on the syringe label.
Reach out to Central Admixture Pharmacy Services, Inc. at 7935 Dunbrook Road, Suite C, San Diego, CA 92126 for more information.
The syringes lack validation data for sanitization cycles, which could result in them not being sterile.
Affected lots include 17-271133, 17-271155, 17-271568, 17-271569, 17-271741, 17-271762, 17-272051, 17-272227, 17-272343, 17-272799, 17-273173, and 17-273495 with specific expiration dates through September 2023.
Check the NDC number on the syringe label; affected syringes have NDC 71286-2071-3 and specific lot numbers with expiration dates from July 2023 through September 2023.
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-1054-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1054-2023 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.
