B. Braun recalls specific batches of Perifix One Epidural Full Tray due to potential catheter connector leakage during use, which may cause disconnection or fluid leakage. Affected units include batch numbers 61588931, 61589445, 61592524, 61609149, 61598518, 61615365, 61619575, 61620760.
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 specific batches of Perifix One Epidural Full Tray devices because the catheter connectors may not stay closed, leading to possible leakage or disconnection of catheters. This could cause fluid leakage during medical procedures, potentially affecting patient safety.
The catheter connectors in the recalled devices may not stay securely closed during use. This can lead to leakage or disconnection of catheters, which might cause fluid leakage during medical procedures. While not immediately dangerous, this risk could impact patient safety if disconnections occur.
Physicians using the Perifix One Epidural Full Tray for anesthetic administration are affected. Those with the specific batch numbers listed in the recall are most at risk.
Check the batch number on the device label. The affected batches are 61588931, 61589445, 61592524, 61609149, 61598518, 61615365, 61619575, and 61620760.
Look for the batch number on the device label to determine if it is affected.
If you have the affected batch numbers, contact B. Braun Medical Inc for further instructions.
The Perifix One Epidural Full Tray with Material Number 332282, specific batch numbers 61588931, 61589445, 61592524, 61609149, 61598518, 61615365, 61619575, and 61620760.
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of catheters.
Check the batch number on the device label. If it matches the affected batches, contact B. Braun Medical Inc 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-3379-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3379-2018 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.
