B. Braun recalls CCE18HK10L epidural trays due to potential catheter connector leakage during use. Affected units have batch number 61595499. Contact for remedy details.
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 because their 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 catheters. This could lead to improper anesthetic delivery if the connector fails while administering anesthesia.
Physicians using the CCE18HK10L epidural tray with batch number 61595499 for anesthesia administration are affected. Those using the device for continuous anesthetic delivery are most at risk.
Check for the product name 'CCE18HK10L CONT EPIDURAL TRAY' with material number 332264. Affected units have batch number 61595499.
Identify the product name and batch number to confirm if your unit is affected.
The catheter connectors may not stay closed during use, which has led to observed leakage or disconnection of catheters in some cases.
The recall record does not specify a remedy, so contact B. Braun Medical for further instructions.
The recall indicates potential leakage or disconnection during use, which could lead to improper anesthetic delivery, but the record does not specify serious injury risk.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3377-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3377-2018 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.
