Degania Medical Devices recalls temperature sensing silicone catheters with potential quality control issues. Affected lot numbers include V18013621 through V19008749. Consumers should contact the company for details.
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 certain temperature sensing silicone catheters due to inadequate quality control during production. This could lead to faulty temperature readings, which might affect medical treatment decisions.
The catheters were produced with thermistor sensors that may have been improperly inspected, potentially causing inaccurate temperature readings. This could lead to incorrect medical assessments if the catheter is used for temperature monitoring during urinary drainage.
Patients using the recalled catheters for urinary drainage. Healthcare providers who use these catheters for medical monitoring are also at risk.
Check the product label for lot numbers: V18013621, V18014635, V18025989, V18029252, V18032217, V18031184, V19006387, V18049356, V18049355, or V19008749. The product is a 3 lumen silicone catheter with a temperature sensor for urinary drainage.
Look for lot numbers on the catheter label: V18013621 through V19008749.
The catheters were produced with thermistor sensors that may have been improperly inspected, potentially causing inaccurate temperature readings.
Check the product label for lot numbers: V18013621, V18014635, V18025989, V18029252, V18032217, V18031184, V19006387, V18049356, V18049355, or V19008749.
Contact Degania Medical Devices for instructions on how to handle the recalled product.
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-1785-2020 — Degania Medical Devices Degania Medical Devices Hello, I own a Degania Medical Devices that is covered by recall Z-1785-2020 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.
