Braun recalls four micro-introducer kits with potential open seal in sterile packaging. Affected kits have specific model numbers and lot codes. Consumers should contact Braun for details.
Due to a potential open seal in the sterile barrier packaging .
Braun is recalling four specific micro-introducer kits due to a potential open seal in the sterile packaging. This could compromise the sterility of the medical device during use, posing a risk of infection.
The sterile packaging may have an open seal, which could allow contamination of the medical device. This might lead to infection if the device is used without proper sterility.
Healthcare professionals who use these kits for vascular procedures may be affected. Those with the specific model numbers and lot codes listed are most at risk.
Check for model numbers KIT-018-47, KIT-019-67, KIT-018-41, or KIT-019-37 on the packaging. Also look for the corresponding lot numbers and UDI-DI codes listed in the recall notice.
Identify the model number and lot code on the packaging to confirm if it is affected.
The sterile packaging may have an open seal, which could allow contamination of the device.
Check for model numbers KIT-018-47, KIT-019-67, KIT-018-41, or KIT-019-37 on the packaging.
Contact Braun directly for further instructions as the recall remedy is not specified in the notice.
We’ve drafted a message you can send Braun to request your refund or repair — edit it as you like.
Subject: Recall Z-1732-2025 — Braun Braun Hello, I own a Braun that is covered by recall Z-1732-2025 from 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.
