[Recalled] Temperature Sensor Catheter 16FR, Catalogue Number 102201101663BI 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 draina
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| Product | Temperature Sensor Catheter 16FR, Catalogue Number 102201101663BI 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 monit |
|---|---|
| Brand / manufacturer | Degania Silicone, Ltd. |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2761-2018 |
| Country of notice | Israel |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 21 June 2018 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in Israel and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Degania Silicone, Ltd.
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.