B. Braun recalls specific epidural basic tray models due to potential catheter connector leakage. Affected units may cause disconnection during use. Consumers should contact manufacturer 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 certain epidural basic trays that may leak or disconnect during use. This could lead to improper anesthetic delivery if the catheter becomes disconnected.
The catheter connectors in these trays may not stay closed properly during use. This can lead to leakage or disconnection of the catheter from the connector, potentially causing improper anesthetic delivery.
Physicians using the recalled epidural basic trays for anesthetic administration are affected. Those with the specific batch numbers listed in the recall are most at risk.
Check for the model CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY with Material Number 332077. Affected units have batch numbers: 61595534, 61596125, 61601680, 61604904, 61607912, 61607913, 61607914, 61607915, 61607911, 61607916, 61607917, 61607918, 61607921, 61609180, 61610345, 61607922, 61607919, 61607920.
Identify the model CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY with Material Number 332077 and affected batch numbers.
Reach out to B. Braun Medical, Inc. for specific instructions on handling the recalled item.
The recalled model is CE17TBFC EPIDURAL BASIC TRAY 17G TOUHY with Material Number 332077.
Affected batch numbers include 61595534, 61596125, 61601680, 61604904, 61607912, 61607913, 61607914, 61607915, 61607911, 61607916, 61607917, 61607918, 61607921, 61609180, 61610345, 61607922, 61607919, 61607920.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of the catheters.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3331-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3331-2018 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.
