B. Braun recalls certain pain management trays with material numbers 530029-555987 for potential catheter connector leakage or disconnection during use.
The catheter connectors may not stay closed during in and in some cases, leakage or disconnection of the catheters from the catheter connectors has been observed.
B. Braun is recalling specific pain management trays that may have catheter connectors which don't stay closed, potentially causing leaks or disconnections. This could lead to improper administration of anesthetic fluids during medical procedures.
The catheter connectors in these trays may not stay securely closed during use. This can lead to leakage or disconnection of catheters from the connectors, which might cause improper administration of anesthetic fluids during medical procedures.
Healthcare professionals using the recalled trays for administering anesthetic fluids are most at risk. Patients receiving procedures with these trays could experience complications from improper fluid delivery.
Check for material numbers starting with 530029, 530031, 530035, 530041, 530048, 530068, 530071, or other numbers listed in the recall notice. The product is a pain management tray used by physicians for anesthetic administration.
Identify the material number on your tray to see if it matches the recalled list (e.g., 530029, 530031, 530035, etc.).
Reach out to B. Braun Medical Inc. for further instructions if you have a recalled tray.
The catheter connectors may not stay closed during use, which can cause leakage or disconnection of catheters from the connectors.
Check the material number on your tray; recalled models include numbers like 530029, 530031, 530035, and others listed in the recall notice.
Contact B. Braun Medical Inc. for instructions on next steps, as the recall does not include a specific remedy.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3404-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3404-2018 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.
