Central Admixture Pharmacy Services recalls rocuronium 50mg/5mL syringes due to lack of sterility assurance. Affected lots expire through August 2023. Consumers should not use these syringes.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services has recalled rocuronium 50mg/5mL syringes that were repackaged by their company. The product lacks proper sterility assurance, which could lead to infections if used.
The syringes were repackaged by Central Admixture Pharmacy Services without sufficient validation of their decontamination cycles. This lack of sterility assurance could introduce contaminants into the drug, potentially causing infections.
Healthcare professionals and patients who use these syringes for medical treatments. Those administering the drug via these syringes are at risk of infection.
Check for lot numbers 36-238805 through 36-252323 on the syringe packaging. These syringes were repackaged by CAPS Inc and expire through August 2023.
Look for lot numbers 36-238805 through 36-252323 on the syringe packaging.
These syringes lack sterility assurance and should not be used for medical treatments.
The product is rocuronium 50mg/5mL syringes repackaged by Central Admixture Pharmacy Services, Inc. with specific lot numbers.
The syringes lack sufficient validation of decontamination cycles, which could lead to contamination and infection.
Check for lot numbers 36-238805 through 36-252323 on the syringe packaging. These syringes expire through August 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-0947-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0947-2023 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.
