Degania Silicone recalls temperature sensor catheters that may show inaccurate low body temperatures during surgery. Affected units have specific catalogue numbers and were sold for medical use.
The catheters are suspected to contain defective sensors; if used, defective catheter will show lower body temperature than the actual body temperature of a patient.
Degania Silicone is recalling temperature sensor catheters that may show lower body temperature readings than actual patient temperatures. This could lead to incorrect medical decisions during surgery or post-surgical care.
The catheters contain defective temperature sensors that may display lower body temperatures than actual patient temperatures. This could cause medical staff to make incorrect decisions about patient health during critical procedures.
Healthcare professionals using the catheters for surgical temperature monitoring are most at risk. Patients undergoing surgery or post-surgical care with these catheters may experience inaccurate temperature readings.
Check for the catalogue number 102201101063BI on the catheter packaging. These catheters were sold for medical use and have specific model identifiers like V17017035 or V17014151.
Look for the catalogue number 102201101063BI on the catheter packaging or label.
The catheters are suspected to contain defective sensors that may show lower body temperature readings than actual patient temperatures during use.
The recall record does not specify a remedy or action steps for affected users.
Yes, the catalogue number 102201101063BI is associated with this recall, and model identifiers like V17017035 or V17014151 are listed.
We’ve drafted a message you can send Degania Silicone to request your refund or repair — edit it as you like.
Subject: Recall Z-2758-2018 — Degania Silicone Degania Silicone Hello, I own a Degania Silicone that is covered by recall Z-2758-2018 from Degania Silicone. 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.
