B. Braun recalls CE18TIN CONT EPIDURAL SET LF (Material 332201) due to potential catheter connector leakage during use. Affected units include specific batch numbers sold for medical anesthesia 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 a specific epidural set model because its catheter connectors can leak or disconnect during use. This could lead to improper anesthetic delivery if the connector fails while administering anesthesia.
The catheter connectors may not stay closed during use, which can cause leakage or disconnection of the catheter from the connector. This could result in improper anesthetic delivery if the connector fails while administering anesthesia.
Physicians using the CE18TIN CONT EPIDURAL SET LF for anesthesia delivery are affected. Those with the specific batch numbers listed are most at risk.
Check for the model CE18TIN CONT EPIDURAL SET LF with Material Number 332201. Affected units include batch numbers 61614720 and 61622724.
Identify the model CE18TIN CONT EPIDURAL SET LF with Material Number 332201 and batch numbers 61614720 or 61622724.
The catheter connectors may not stay closed during use, which can cause leakage or disconnection of the catheter from the connector.
Check if your product matches the model CE18TIN CONT EPIDURAL SET LF with Material Number 332201 and batch numbers 61614720 or 61622724. If it does, 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-3351-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3351-2018 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.
