B. Braun recalls CNB200TK nerve block devices with material number 331701 due to potential catheter connector leakage. Affected units include specific batches sold to medical facilities. Contact for return instructions.
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 nerve block devices that may leak or disconnect during use, which could lead to improper medication delivery. This recall affects medical facilities using specific batch numbers of the CNB200TK device.
The catheter connectors in these devices may not stay closed during use, leading to potential leakage or disconnection of the catheter from the connector. This could cause improper medication delivery or infection risks during procedures.
Medical facilities that purchased the CNB200TK nerve block device with material number 331701 are likely affected. Physicians using these devices for anesthetic administration are at risk if the connectors leak or disconnect.
Check for the product name 'CNB200TK CONTIPLEX CONT NERVE BLOCK' with material number 331701. Affected units include specific batches: 61598523, 61601873, and 61611463.
Identify if your device has batch numbers 61598523, 61601873, or 61611463.
Reach out to B. Braun Medical, Inc. for return or repair instructions.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheter from the connector.
Batches 61598523, 61601873, and 61611463.
Look for the product name 'CNB200TK CONTIPLEX CONT NERVE BLOCK' with material number 331701 and the specific batch numbers listed.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3323-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3323-2018 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.
