Central Admixture Pharmacy Services recalls hydro morphine syringes due to lack of validation data for 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 hydro morphine syringes that may not be sterile due to insufficient sanitization validation. This could lead to infections if used improperly.
The syringes lack validated sanitization cycles, meaning they might not be sterile. If used without proper sterilization, this could cause infections in patients.
Healthcare professionals and patients using these syringes for medical purposes. Those with the specific lot numbers listed in the recall are most at risk.
Check the lot numbers on the syringe packaging: 17-270675, 17-270683, 17-271147, 17-271119, 17-271339, 17-271679, 17-272202, 17-272241, 17-272375, 17-272783, 17-273438, 17-273431, 17-273615, 17-273789. The expiration dates range from July 2023 to September 2023.
Look for lot numbers on the syringe packaging: 17-270675, 17-270683, 17-271147, 17-271119, 17-271339, 17-271679, 17-272202, 17-272241, 17-272375, 17-272783, 17-273438, 17-273431, 17-273615, 17-273789.
The syringes lack validated sanitization cycles, which means they may not be sterile and could cause infections if used improperly.
Lots 17-270675, 17-270683, 17-271147, 17-271119, 17-271339, 17-271679, 17-272202, 17-272241, 17-272375, 17-272783, 17-273438, 17-273431, 17-273615, 17-273789.
Check the lot numbers on the syringe packaging; affected lots have specific numbers 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-1049-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1049-2023 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
