B. Braun recalls EPID trays with potential catheter connector leakage. Affected units have batch number 61580395. Stop using if leakage occurs.
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 a specific type of medical tray used by doctors that may leak or disconnect during use. This could lead to improper medication delivery or infection risks if the tray isn't sealed properly.
The catheter connectors may not stay closed during use, causing leakage or disconnection of catheters. This could lead to improper medication delivery or infection risks if the tray isn't sealed properly.
Physicians using the recalled EPID tray for anesthesia administration are most at risk. The specific batch number 61580395 is affected.
Check for the batch number 61580395 on the tray. The product is a medical tray used by doctors for anesthesia and fluid administration.
If the connector leaks or disconnects during use, stop using the tray immediately.
The recall indicates potential leakage or disconnection, so it's not safe to use without checking for issues.
Batch number 61580395 is affected.
Look for the batch number 61580395 on the tray, which is used by doctors for anesthesia and fluid administration.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3341-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3341-2018 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.
