FDA Enforcement
Class II
Terminated
Thermistor Foley catheter, nonsterile, Catalogue Number 102201101463MD Product Usage: This is sterile, single use, two-way silicone Foley Catheter with a thermistor embedded in the third lumen. It is intended for use in the drainage/ collection of urine from the urinary bladder and simultaneous monitoring of the body core temperature during surgery or post-surgical period.
Recall: Z-2780-2018
·
Reported September 26, 2018
Enforcement
- Recall Number
- Z-2780-2018
- Event ID
- 80641
- Classification
- Class II
- Status
- Terminated
- Product Type
- Devices
- Firm
- Degania Silicone, Ltd.
- Voluntary / Mandated
- Voluntary: Firm initiated
- Initial Notification
- Letter
- Report Date
- September 26, 2018
- Initiation Date
- June 21, 2018
- Classification Date
- September 20, 2018
- Termination Date
- October 25, 2024
- Address
- Degania Bet, N/A, Dganya Bet, N/A, N/A, Israel
Description
Thermistor Foley catheter, nonsterile, Catalogue Number 102201101463MD Product Usage: This is sterile, single use, two-way silicone Foley Catheter with a thermistor embedded in the third lumen. It is intended for use in the drainage/ collection of urine from the urinary bladder and simultaneous monitoring of the body core temperature during surgery or post-surgical period.
Reason
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.
Code Info
V17023217, V17028046, V17028047
Distribution
Worldwide Distribution - US Nationwide in the states: IL, NC, NY and the countries of : Belgium, Israel, Japan, and Mexico.
Quantity
3885