Degania Silicone recalls sterile temperature-sensing catheters that may display lower body temperature than actual. Patients at risk during surgery or post-surgery care.
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 incorrect temperature monitoring during surgery or after surgery, potentially affecting patient care.
The catheters contain defective temperature sensors that may show lower body temperature than the actual temperature. This could lead to incorrect temperature readings during critical medical procedures, potentially affecting patient care decisions.
Patients undergoing surgery or post-surgical care who use these catheters for temperature monitoring are most at risk. Healthcare providers using the product for temperature monitoring during medical procedures are affected.
Look for the product name 'Temperature Sensing 100% Silicone Foley Catheter, sterile' with catalogue number 102201101880MD. These were sold for use in surgery or post-surgical care.
Verify the product name and catalogue number to confirm if you have the recalled item.
The catheters are suspected to contain defective sensors that may show lower body temperature than actual, which could affect temperature monitoring during surgery or post-surgical care.
The recall record does not specify a remedy, so check the product details to confirm if you have the recalled item.
The recall does not mention a risk of serious injury; it focuses on potential incorrect temperature readings 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-2774-2018 — Degania Silicone Degania Silicone Hello, I own a Degania Silicone that is covered by recall Z-2774-2018 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.
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.
