B. Braun Medical recalls Potassium Chloride for Injection Concentrate due to potential pinholes causing leaks. This affects specific lots and expiration dates. Consumers should contact the company for details.
Lack of assurance of sterility: pinholes, within the blue label characters on the EXCEL bag, specifically within the dotted characters on the label, resulting in leaks.
B. Braun Medical is recalling Potassium Chloride for Injection Concentrate because pinholes in the packaging could cause leaks. This poses a risk of contamination during medical use, which could lead to serious health issues if not addressed.
The packaging has pinholes that can leak, potentially causing contamination. This contamination could lead to infections or other health complications if the product is used improperly.
Healthcare professionals and patients who have received the specific lot numbers of Potassium Chloride for Injection Concentrate. Those using the product for medical purposes are most at risk.
Check the product label for the lot numbers J2S007 (expiring 12/31/2024) or J3A115 (expiring 01/31/2025). The product is a 250 mL bag of Potassium Chloride for Injection Concentrate, 500 mEq/250 mL, sold by B. Braun Medical.
Look for the lot numbers J2S007 (expiring 12/31/2024) or J3A115 (expiring 01/31/2025) on the packaging.
Potassium Chloride for Injection Concentrate USP, 500 mEq/250 mL (2 mEq/mL), 250 mL Bag, Rx only, manufactured by B. Braun Medical.
Check the product label for lot numbers J2S007 (expiring 12/31/2024) or J3A115 (expiring 01/31/2025).
The recall record does not specify a remedy, so contact B. Braun Medical directly for instructions.
We’ve drafted a message you can send B. Braun Medical to request your refund or repair — edit it as you like.
Subject: Recall D-0370-2024 — B. Braun Medical B. Braun Medical Hello, I own a B. Braun Medical that is covered by recall D-0370-2024 from B. Braun Medical. 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.
