CLASS II Device recall · Reported 29 Apr 2020 · FDA Enforcement Report
Temperature Sensing 100% Silicone Foley Catheter recalled
Degania Medical Devices is recalling Temperature Sensing 100% Silicone Foley Catheter, distributed nationwide in the US. The recall was initiated on 17 Mar 2020 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1779-2020
- FDA event ID
- 85327
- Recalling firm
- Degania Medical Devices, Gurgaon, N/A
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 17 Mar 2020
- FDA classified
- 23 Apr 2020
- Reported
- 29 Apr 2020
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Temperature Abuse
- Device type
- Heart & Vascular Devices
Timeline
| 17 Mar 2020 | Recall initiated by company | |
| 23 Apr 2020 | Classified by FDA | +37 days |
| 29 Apr 2020 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Inadequate incoming inspection practices were utilized on thermistor sensors used in the production of the specified lots of temperature sensing catheters.
Foods that need refrigeration and were stored or shipped too warm can grow harmful bacteria without any change in look or smell.
Product as listed by the FDA
Temperature Sensing 100% Silicone Foley Catheter, Part Number 102201100880MD - Product Usage: is a 3 lumen silicone catheter with a sensor to measure temperature while draining the urinary bladder.
Where it was distributed
Worldwide distribution - US Nationwide distribution including state of IL and the country of Mexico.
Questions about this recall
Why was it recalled?
Inadequate incoming inspection practices were utilized on thermistor sensors used in the production of the specified lots of temperature sensing catheters.
Which lots are affected?
Lot Numbers: S18013318 S18010936 S19006220 S19006221 S19006222 S19006349
Where was it sold?
Worldwide distribution - US Nationwide distribution including state of IL and the country of Mexico.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
10 other products · FDA event 85327More recalls from Degania Medical Devices
All 11| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Temperature Sensing 100% Silicone Foley Catheter recalled | Degania Medical Devices | Temperature Abuse | Nationwide |
| Device | CLASS II | Temperature Sensing 100% Silicone Foley Catheter recalled | Degania Medical Devices | Temperature Abuse | Nationwide |
| Device | CLASS II | Temperature Sensing 100% Silicone Foley Catheter recalled | Degania Medical Devices | Temperature Abuse | Nationwide |
| Device | CLASS II | Temperature Sensing 100% Silicone Foley Catheter recalled | Degania Medical Devices | Temperature Abuse | Nationwide |
| Device | CLASS II | Temperature Sensing 100% Silicone Foley Catheter recalled | Degania Medical Devices | Temperature Abuse | Nationwide |
Other Heart & Vascular Devices recalls
All 6,199| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Getinge PVC Thoracic Catheter, Soft PVC Right Angle recalled | Atrium Medical | Potency & Assay | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes: *Bardex¿ I.C recalled | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Products that contain the Pericare Wipes recalled by C.R. Bard | C.R. Bard | Other | Nationwide |
| Device | CLASS II | Getinge PVC Thoracic Catheter, Firm PVC Straight recalled | Atrium Medical | Potency & Assay | Nationwide |