B. Braun recalls specific epidural trays with potential catheter connector leakage. Affected units have batch numbers listed. Stop using if you have the model and batch numbers.
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 epidural trays that may leak or disconnect during use. This could lead to improper anesthetic delivery and potential complications for patients under medical procedures.
The catheter connectors in these trays may not stay securely closed during use. This can cause leakage or disconnection of the catheter, potentially leading to improper anesthetic delivery and patient complications.
Physicians using the recalled epidural trays for anesthetic administration are most at risk. Patients receiving procedures with these trays may face complications if the catheter disconnects.
Check for the model CE17TKFC with batch numbers: 61588411, 61589132, 61590240, 61591302, 61591816, 61592013, 61592513, 61594212, 61595169, 61595496, 61596322, 61596323, 61597455, 61597456, 61618678, 61614704, 61618680, 61618681, 61621829, 61621830, 61587111, 61587112.
Identify if your epidural tray has the model CE17TKFC and one of the listed batch numbers.
If you have the recalled model and batch numbers, stop using the tray immediately to prevent potential leakage or disconnection.
The model number is CE17TKFC with batch numbers listed in the recall notice.
Check for the model CE17TKFC and one of the batch numbers: 61588411, 61589132, 61590240, 61591302, 61591816, 61592013, 61592513, 61594212, 61595169, 61595496, 61596322, 61596323, 61597455, 61597456, 61618678, 61614704, 61618680, 61618681, 61621829, 61621830, 61587111, 61587112.
The recall notice does not specify a return process, but you should stop using it if it's affected.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3333-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3333-2018 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.
