B. Braun recalls specific batches of EPID trays with 17G Tuohy-LF catheter connectors due to potential leakage or disconnection during use, which could lead to anesthetic fluid administration issues.
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 certain batches of EPID trays with 17G Tuohy-LF catheter connectors because they may leak or disconnect during use. This could cause anesthetic fluids to be administered improperly, risking patient safety.
The catheter connectors may not stay closed properly, leading to leakage or disconnection of catheters. This could result in improper administration of anesthetic fluids during medical procedures.
Physicians using the recalled EPID trays for anesthetic and fluid administration are affected. Those handling the specific batch numbers listed in the recall are most at risk.
Check for the model CE17TKFCS with batch numbers 61588414, 61587114, 61590499, and other listed batches. The product is a catheter connector used by physicians for anesthetic delivery.
Identify the batch number on the product label to determine if it is in the recalled list.
Reach out to B. Braun Medical for guidance on next steps if the product is recalled.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of catheters, which could cause improper anesthetic fluid administration.
The affected batch numbers include 61588414, 61587114, 61590499, 61591305, 61591822, and others listed in the recall notice.
The recall record does not specify a remedy, so users should contact B. Braun Medical for further instructions.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3343-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3343-2018 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.
