B. Braun recalls Perifix/epidural anesthesia kits with incorrect filter straw. Affected kits may cause complications during surgery. Return or stop use immediately.
Kits were assembled with the incorrect Filter Straw.
B. Braun is recalling Perifix/epidural anesthesia kits that were assembled with the wrong filter straw. This could lead to complications during surgery if the kit is used.
The kits were assembled with the incorrect filter straw, which could cause complications during surgery. This error might lead to improper fluid flow or contamination risks.
Healthcare providers using the recalled Perifix/epidural anesthesia kits are most at risk. Patients undergoing surgery with these kits may face complications.
Check for model numbers 332217, 332097, 332220, or 332078 on the carton. The kits were sold with specific lot numbers including 0061850767.
Verify the model number on the carton to see if it matches the recalled models (332217, 332097, 332220, 332078).
Reach out to B. Braun Medical Inc for guidance on next steps if the kit is affected.
The kits were assembled with the incorrect filter straw, which could cause complications during surgery.
Check for model numbers 332217, 332097, 332220, or 332078 on the carton. The kits were sold with specific lot numbers including 0061850767.
Contact B. Braun Medical Inc for guidance on next steps if the kit is affected.
We’ve drafted a message you can send B. Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-2002-2023 — B. Braun B. Braun Hello, I own a B. Braun that is covered by recall Z-2002-2023 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.
