Central Admixture Pharmacy Services recalls Sutter Cardioplegia Solution (25 mEq K, 572.64 mL IV bag) due to lack of sterility assurance. This product is for central line use only and may cause infections if not properly sterilized.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services recalls Sutter Cardioplegia Solution (25 mEq K, 572.64 mL IV bag) because it lacks proper sterility validation. This poses a risk of infection for patients receiving intravenous treatments.
The solution may not be sterile due to insufficient validation of decontamination cycles. This can lead to infections in patients receiving intravenous treatments through central lines.
Healthcare professionals using this solution for central line procedures. Patients receiving intravenous treatments with this product are at risk of infection.
Check for the product name 'Sutter Cardioplegia Solution', 25 mEq K, 572.64 mL IV bag. The lot number 36-253947 and expiration date 7/20/2023 are specific identifiers.
Verify the lot number and expiration date on the product label to confirm if it matches the recalled batch.
The product is not safe for use as it lacks sterility validation, which could lead to infections.
Look for the product name 'Sutter Cardioplegia Solution', 25 mEq K, 572.64 mL IV bag with lot number 36-253947 and expiration date 7/20/2023.
The recall does not specify a remedy, so contact the manufacturer for further instructions.
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-1021-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1021-2023 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.
