B. Braun recalls ACCU-BLOC PERIFIX Kit (Material 332230) due to potential catheter leakage. Affected units may leak or disconnect during anesthesia administration. Contact for return instructions.
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 a specific anesthetic kit that may leak or disconnect during use, which could lead to improper anesthesia delivery. Patients and healthcare providers should stop using the affected kits to prevent potential complications.
The catheter connectors in this kit may not stay securely closed, leading to leakage or disconnection of the catheter during anesthesia procedures. This could cause improper delivery of anesthetic fluids to patients.
Healthcare providers using the ACCU-BLOC PERIFIX Kit for anesthesia administration are most at risk. The recall affects units sold with batch number 61596062.
Check for the model CE18HK ACCU-BLOC PERIFIX Kit with Material Number 332230. Affected units were sold with batch number 61596062.
Verify the model number (CE18HK) and batch number (61596062) to confirm if your kit is affected.
Reach out to B. Braun Medical for specific return or replacement instructions.
The recall indicates potential leakage or disconnection risks, so affected kits should not be used until resolved.
Check the batch number and contact B. Braun Medical for return or replacement instructions.
The recall specifies batch number 61596062, but the exact number of affected units is not stated in the record.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-3368-2018 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-3368-2018 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.
