B. Braun recalls 3000mL sterile water for injection due to potential fluid leakage from port misalignment. Affected lots expire by August 2026 and February 2027. Stop using immediately if you have this product.
Lack of Assurance of Sterility- Potential for fluid leakage from the port due to port misalignment.
B. Braun is recalling sterile water for injection (3000mL, Rx only) because it may leak from the port due to misalignment. This could lead to contamination or infection if used improperly. The recall affects specific lots with expiration dates up to February 2027.
The product may leak from the port if misaligned, which could cause contamination or infection during medical procedures. This risk is specific to the port design and handling conditions.
Healthcare professionals and patients who use this sterile water for medical injections. Those with the specific lot numbers listed are most at risk.
Check the lot number on the label: J3L519, J3L528 (expiring August 2026) or J4C522, J4C523 (expiring February 2027). This product is only for prescription use in medical settings.
Look for lot numbers J3L519, J3L528 (expiring August 2026) or J4C522, J4C523 (expiring February 2027) on the label.
The product is not safe for use as recalled due to potential fluid leakage from port misalignment. Do not use until the recall is resolved.
Check the lot number on the label. If it matches the recalled lots, stop using it immediately and contact B. Braun for instructions.
The recall covers specific lots expiring by August 2026 and February 2027. The exact duration depends on when the product was manufactured and used.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall D-0652-2025 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall D-0652-2025 from B. Braun. 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.
