Central Admixture Pharmacy Services recalls potassium phosphate 30 mmole in 0.9% sodium chloride 500mL bags due to potential sterility issues found during FDA inspection. These products are for medical use only and must be discarded if used.
Lack of Assurance of Sterility: after an FDA inspection called into question the sterility of the products intended to be sterile.
Central Admixture Pharmacy Services is recalling specific potassium phosphate solutions that were found to lack sterility during an FDA inspection. This means the products could cause infections if used in medical procedures.
The FDA inspection found that the products intended to be sterile were not properly sterilized. This could lead to infections in patients receiving the solution through intravenous lines.
Healthcare professionals who use these products for medical procedures are affected. Patients receiving these solutions through IV lines are at risk of infection.
Check for the product name 'potassium phosphate 30 mmole added to 0.9% sodium chloride 500 mL per bag'. Look for lot numbers 37-883219 through 37-894987 with expiration dates up to May 2023.
Immediately discard any unused products as they may cause infections if used in medical procedures.
The FDA found that the products intended to be sterile were not properly sterilized during manufacturing.
Discard the product immediately and do not use it for medical procedures.
Yes, check for lot numbers 37-883219 through 37-894987 with expiration dates up to May 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-0728-2023 — Central Admixture Pharmacy Services Central Admixture Pharmacy Services Hello, I own a Central Admixture Pharmacy Services that is covered by recall D-0728-2023 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.
