Vital Signs Devices, a GE Healthcare recalls
Vital Signs Devices, a GE Healthcare has 3 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 21 Aug 2013. The most frequent reason is sterility.
Total recalls3since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 21 Aug 2013
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 3 100%Class III 0 0%
Why vital signs devices, a ge healthcare is recalled
Product types
By year
All vital signs devices, a ge healthcare recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Disposable Temperature Probes, (sterile), Sensor diameter recalled | Vital Signs Devices, a GE Healthcare | Sterility | Nationwide |
| Device | CLASS II | Corometrics Qwik Connect Plus Spiral Electrode recalled | Vital Signs Devices, a GE Healthcare | Packaging Defects | Nationwide |
| Device | CLASS II | enFlow IV Fluid Warmer (510k name: Eflow IV Fluid Warmer recalled | Vital Signs Devices, a GE Healthcare | Device Malfunction | Nationwide |
About this list
Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.