Central Admixture Pharmacy Services recalls specific HYDROmorphone syringes (NDC 71286-2012-1) due to lack of sterility assurance from sanitization cycles. Affected units have specific lot numbers and expiration dates.
Lack of assurance of sterility: Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling certain HYDROmorphone syringes because they may not be sterile due to insufficient validation of their sanitization cycles. This could lead to infections if the medication is used without proper sterility.
The syringes lack sufficient validation data for their sanitization cycles, meaning they may not be sterile. This could lead to infections if the medication is administered without proper sterility.
Healthcare professionals using these syringes for prescription medication preparation are most at risk. Patients receiving the medication through these syringes could be affected if the syringes are not sterile.
Check for the NDC number 71286-2012-1 on the syringe label. Affected units have specific lot numbers and expiration dates listed in the recall notice.
Look for the NDC number 71286-2012-1 and specific lot numbers listed in the recall notice.
The recall indicates a lack of sterility assurance, so these syringes should not be used until the manufacturer provides a remedy.
Check the syringe label for the NDC number 71286-2012-1 and specific lot numbers listed in the recall notice. If affected, contact the manufacturer for guidance.
The recall lists specific lot numbers and expiration dates. Check your syringe label for these details.
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-1060-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1060-2023 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.
