B. Braun recalls CE17TB19C epidural trays with material number 332242 due to potential catheter connector leakage during use. Affected units include specific batch numbers sold for medical anesthetic delivery.
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 epidural trays with model CE17TB19C and material number 332:2242 because the catheter connectors may leak or disconnect during use. This could lead to improper anesthetic delivery if the connection fails while a patient is receiving treatment.
The catheter connectors in these trays may not stay securely closed during use, which can cause leakage or disconnection of the catheter from the connector. This could result in improper anesthetic delivery if the connection fails while a patient is receiving treatment.
Physicians using the CE17TB19C epidural trays for anesthetic delivery are most at risk. The recall affects specific batch numbers of the trays sold for medical use.
Check for the model CE17TB19C and material number 332242 on the tray. Affected units include batch numbers 61620798 and 61583520 sold for medical anesthetic delivery.
Inspect the catheter connector for signs of leakage or disconnection during use.
Reach out to B. Braun Medical Inc for guidance on handling affected units.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheter from the connector.
Check for the model CE17TB19C and material number 332242. Contact B. Braun Medical Inc for guidance on handling affected units.
Yes, affected batch numbers are 61620798 and 61583520.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3375-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3375-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
