Degania Medical Devices recalls temperature sensing silicone catheters due to inadequate quality control during production. This may lead to inaccurate temperature readings during urinary drainage. Affected lot V18022032.
Inadequate incoming inspection practices were utilized on thermistor sensors used in the production of the specified lots of temperature sensing catheters.
Degania Medical Devices is recalling temperature sensing silicone catheters that may have inaccurate temperature readings due to production quality control issues. This could affect medical procedures requiring precise temperature monitoring during urinary drainage.
The catheters were produced with thermistor sensors that may not function correctly due to inadequate incoming inspection practices. This could lead to inaccurate temperature readings during urinary drainage procedures, potentially affecting medical decisions.
Patients using the recalled catheters for urinary drainage procedures. Healthcare providers who use these catheters for temperature monitoring are most at risk.
Check for the lot number V18022032 on the catheter packaging. The product is a 3 lumen silicone catheter with a temperature sensor for urinary drainage.
Look for the lot number V18022032 on the catheter packaging to confirm if it's affected.
The recalled catheter is a 3 lumen silicone temperature sensing catheter with part number 102201101063MD.
The recall is due to inadequate incoming inspection practices during production of the thermistor sensors, which could lead to inaccurate temperature readings.
Check for the lot number V18022032 on the catheter packaging. The product is a 3 lumen silicone catheter with a temperature sensor for urinary drainage.
We’ve drafted a message you can send Degania Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-1780-2020 — Degania Medical Devices Degania Medical Devices Hello, I own a Degania Medical Devices that is covered by recall Z-1780-2020 from Degania Medical Devices. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
