B. Braun recalls Accu-Bloc Perifix Kit (Material 332600) due to potential catheter connector leakage during use. Affected units include specific batch numbers sold for medical anesthesia delivery.
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 its Accu-Bloc Perifix Kit (Material Number 332600) because catheter connectors may not stay closed, leading to possible leakage or disconnection during medical procedures. This could cause complications in anesthesia delivery if the kit is used improperly.
The catheter connectors in this kit may not stay securely closed during medical procedures. This can lead to leakage or disconnection of catheters, potentially causing complications in anesthesia administration if the kit is used without proper connection.
Physicians using the Accu-Bloc Perifix Kit for anesthesia delivery are most at risk. The recall affects specific batch numbers sold for medical use.
Check for the product name 'Accu-Bloc Perifix Kit' with Material Number 332600. Affected units include batch numbers 61596329 and 61606959 sold for medical anesthesia delivery.
Identify the batch number on the kit to determine if it is affected (61596329 or 61606959).
The catheter connectors may not stay closed during use, leading to potential leakage or disconnection of catheters.
Batch numbers 61596329 and 61606959.
No, but you should check the batch number to see if it is affected. If it is, contact B. Braun 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-3385-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3385-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
