Central Admixture Pharmacy Services recalls dilTIAZem 125mg/125mL IV bags due to lack of validation data for sanitization cycles. This poses a risk of contamination during IV administration.
Lack of Assurance of Sterility:Lack of validation data for sanitization cycles
Central Admixture Pharmacy Services is recalling dilTIAZem 125mg/125mL IV bags that were added to dextrose 5% solution. The recall is due to insufficient validation data for sanitization cycles, which could lead to contamination during IV administration.
The IV bags lack validated sanitization cycles, meaning the manufacturing process may not ensure sterility. This could lead to contamination during IV administration, potentially causing infections or other complications.
Healthcare professionals using these IV bags for patient treatment are most at risk. Patients receiving IV medication from this product may be affected.
Check for the product name 'dilTIAZem 125mg/125mL (1 mg/mL) added to dextrose 5%', manufactured by Central Admixture Pharmacy Services. Look for lot numbers 36-260048, 36-262174, or 36-262523 with expiration dates up to September 19, 2023.
Identify the product by checking the lot number and expiration date on the IV bag.
The recall is due to lack of validation data for sanitization cycles, which could result in contamination during IV administration.
The official recall notice does not specify a remedy or action steps for affected products.
Yes, check lot numbers 36-260048, 36-262174, or 36-262523 with expiration dates up to September 19, 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-1138-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-1138-2023 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.
