B. Braun recalls specific epidural set models (CE17TO CONT EPIDURAL SET LF) due to potential catheter connector leakage during use. Affected units include batch numbers 61609098, 61620830, and 61592464.
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 sets that may leak or disconnect during use, which could lead to improper anesthetic delivery. This poses a risk of incorrect medication administration to patients during medical procedures.
The catheter connectors in these sets may not stay securely closed, leading to potential leakage or disconnection of the catheter during medical procedures. This could result in improper delivery of anesthetic fluids to patients.
Physicians using the recalled epidural sets for anesthetic administration are affected. Patients receiving procedures with these sets may be at risk if the connector leaks or disconnects.
Check for the model CE17TO CONT EPIDURAL SET LF with Material Number 332204. Affected units include batch numbers 61609098, 61620830, and 61592464.
Identify the batch number on the product label to determine if it matches 61609098, 61620830, or 61592464.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheters from the connectors.
Check the batch number on the product label. If it matches 61609098, 61620830, or 61592464, contact B. Braun for further instructions.
The recall record does not specify a remedy or fix for this issue.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3353-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3353-2018 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.
