Xodus Medical recalls cauterization tip cleaners with potential sterile barrier issues. Affected units include specific lot numbers and model REF 30500. Consumers should check their product details and contact the company for guidance.
The sterile barrier of some devices may have been affected
Xodus Medical is recalling cauterization tip cleaners (REF 30500) due to possible issues with the sterile barrier. This could lead to contamination during medical procedures if the device is not properly sterilized. The recall affects specific production lots and models.
The sterile barrier of some devices may have been compromised, potentially leading to contamination during medical procedures. This could affect the safety of the surgical process if the device is not properly sterilized.
Healthcare professionals using cauterization tip cleaners for electrosurgical procedures are most at risk. The recall applies to specific production lots and models sold under the REF 30500 designation.
Check for the product model REF 30500 and lot numbers listed in the recall notice (e.g., 16DEC19, 17JAN06, etc.). The device is used as an electrosurgical accessory for cauterization procedures.
Look for the model REF 30500 and lot numbers such as 16DEC19, 17JAN06, or others listed in the recall notice.
Xodus Medical is recalling cauterization tip cleaners with model REF 30500.
Affected lot numbers include 16DEC19, 17JAN06, 17JAN06A, 17JAN23, and others listed in the recall notice.
The recall notice does not specify a remedy, so consumers should check with Xodus Medical for further instructions.
We’ve drafted a message you can send Xodus Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-0151-2020 — Xodus Medical Xodus Medical Hello, I own a Xodus Medical that is covered by recall Z-0151-2020 from Xodus Medical. 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.
