Central Admixture Pharmacy Services recalls dilTIAZem 125mg/125mL IV bags due to lack of sterility assurance. This could lead to infections if used in medical settings. Affected lots expire through August 2023.
Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
Central Admixture Pharmacy Services is recalling dilTIAZem 125mg/125mL IV bags that were added to dextrose 5% solution. The bags lack proper sterility validation, which could cause infections if used in medical treatments.
The bags were not properly validated for sterility, meaning they could contain harmful bacteria. This poses a risk of infection if the bags are used in medical procedures, especially in critical care settings.
Healthcare professionals and patients receiving IV treatments with the recalled dilTIAZem bags. Those using the product in medical settings are at risk of infection.
Check for the product name 'dilTIAZem 125mg/125mL (1 mg/mL) added to dextrose 5%'. Look for the lot numbers 36-243946 to 36-256896 and expiration dates through August 2023.
Identify the lot numbers and expiration dates listed in the recall notice to confirm if your bag is affected.
The recall states that the product lacks sterility validation, so it is not safe for medical use. Do not use the product until the recall is resolved.
The recall does not specify a remedy, so contact the manufacturer directly for guidance on safe disposal or alternatives.
Check the lot numbers and expiration dates listed in the recall notice: 36-243946 to 36-256896 with expiration dates 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-0951-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0951-2023 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.
