B. Braun recalls specific batches of ACCU-BLOC Perifix Kit (Material 332220) due to potential catheter connector leakage during use, which may cause disconnection of anesthetic delivery systems.
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 batches of ACCU-BLOC Perifix Kit for possible leakage from catheter connectors. This could lead to disconnection of anesthetic delivery systems during medical procedures, posing a risk of incorrect medication administration.
The catheter connectors in the recalled kits may not stay closed during use, leading to potential leakage or disconnection of catheters. This could cause anesthetic delivery systems to become disconnected during medical procedures, potentially leading to incorrect medication administration.
Physicians using the recalled ACCU-BLOC Perifix Kit for anesthetic delivery are affected. Those with the specific batch numbers listed in the recall are most at risk.
Check the batch numbers on the kit: 61595170, 61595613, 61596536, 61598356, 61597084, 61600180, 61617168, 61616702, 61617169, 61616703, 61614599, 61616701, 61616700, 61614596, 61614598, 61619583, 61620763, 61622163, 61621828.
Identify the batch numbers on the ACCU-BLOC Perifix Kit to see if they match the listed numbers: 61595170, 61595613, 61596536, 61598356, 61597084, 61600180, 61617168, 61616702, 61617169, 61616703, 61614599, 61616701, 61616700, 61614596, 61614598, 61619583, 61620763, 61622163, 61621828.
B. Braun is recalling specific batches of ACCU-BLOC Perifix Kit (Material Number 332220) due to potential leakage from catheter connectors, which may cause disconnection of anesthetic delivery systems.
Check the batch numbers on the kit: 61595170, 61595613, 61596536, 61598356, 61597084, 61600180, 61617168, 61616702, 61617169, 61616703, 61614599, 61616701, 61616700, 61614596, 61614598, 61619583, 61620763, 61622163, 61621828.
The recall does not specify a remedy, so contact B. Braun Medical, Inc. for further instructions on how to handle the product.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3362-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3362-2018 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.
