Degania Silicone recalls sterile temperature sensing catheters that may display lower body temperature than actual. This could affect surgical monitoring accuracy. Contact for remedy details.
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 sterile temperature sensing catheters that may show lower body temperature than actual. This could lead to inaccurate surgical monitoring, potentially affecting patient care.
The catheters contain defective temperature sensors that may register lower body temperatures than actual. This could cause inaccurate monitoring during critical medical procedures, potentially leading to incorrect treatment decisions.
Healthcare professionals using these catheters during surgery or post-surgical care are most at risk. Patients undergoing procedures requiring temperature monitoring may be affected.
Look for the product name 'Temperature Sensing 100% Silicone Foley Catheter', sterile, with catalogue number 102201101680MD. These were sold for surgical use.
Verify if your catheter has the catalogue number 102201101680MD and is sterile.
The catheters may contain defective sensors that show lower body temperature than actual, potentially affecting surgical monitoring.
The recall record does not specify a remedy, so contact Degania Silicone directly for instructions.
The recall indicates a potential issue with temperature accuracy, so use with caution during medical procedures.
We’ve drafted a message you can send Degania Silicone to request your refund or repair — edit it as you like.
Subject: Recall Z-2775-2018 — Degania Silicone Degania Silicone Hello, I own a Degania Silicone that is covered by recall Z-2775-2018 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.
