B. Braun recalls ES1827K spinal epidural trays with material number 333192 due to potential catheter connector leakage. Affected units include specific batch numbers. Consumers should contact B. Braun for 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 spinal epidural trays that may leak or disconnect catheters during use. This could lead to improper anesthetic delivery and potential complications for patients receiving surgery.
The catheter connectors may not stay closed during use, leading to leakage or disconnection of catheters. This could cause improper anesthetic delivery and potential complications during surgery.
Physicians using the ES1827K spinal epidural trays with material number 333192 are affected. Patients undergoing surgery with this device are at risk of improper anesthetic delivery.
Check for the model ES1827K SPINAL/EPIDURAL TRAY (LF) with material number 333192. Affected units include specific batch numbers: 61592518, 61600751, 61596330, 61603763, 61608873, 61612141, 61615216, 61619581, 61617800, 61621835.
Identify the model ES1827K SPINAL/EPIDURAL TRAY (LF) with material number 333192 and affected batch numbers.
The recalled device is the ES1827K SPINAL/EPIDURAL TRAY (LF) with material number 333192.
Affected batch numbers are 61592518, 61600751, 61596330, 61603763, 61608873, 61612141, 61615216, 61619581, 61617800, and 61621835.
The recall record does not specify a remedy, so contact B. Braun Medical for further instructions.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3391-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3391-2018 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.
