Central Admixture Pharmacy Services recalls repackaged rocuronium 50mg/5mL syringes due to unvalidated sanitization cycles. Affected lots expire 10/11/2023. Consumers should contact CAPS for details.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling repackaged rocuronium 50 mg/5 mL syringes because their sanitization cycles weren't properly validated. This could lead to contamination if the syringes are used in medical procedures.
The syringes were repackaged by CAPS Inc without validated sanitization cycles. This means the syringes might not be sterile, potentially causing infections during medical procedures.
Healthcare professionals using these syringes for medical procedures. Patients receiving injections with these syringes are at risk of infection.
Check for lot numbers 36-262729 through 36-262982 on the syringe packaging. These syringes were sold with expiration date 10/11/2023.
Reach out to Central Admixture Pharmacy Services at 2200 South 43rd Avenue, Phoenix, AZ for specific recall details and instructions.
The recall states there is a lack of validation for sanitization cycles, so these syringes may not be sterile. Do not use them until contacting CAPS.
Contact Central Admixture Pharmacy Services at 2200 South 43rd Avenue, Phoenix, AZ for instructions on what to do with the recalled syringes.
Look for lot numbers 36-262729 through 36-262982 on the syringe packaging. These syringes expire 10/11/2023.
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-1113-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1113-2023 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.
