Ellipse A/S recalls
Ellipse A/S has 2 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 15 Jun 2016. The most frequent reason is device malfunction.
Total recalls2since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 15 Jun 2016
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 2 100%Class III 0 0%
Why ellipse a/s is recalled
Product types
By year
All ellipse a/s recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | ND: YAG Laser applicator for Ellipse Nordlys system Medical recalled | Ellipse A/S | Device Malfunction | Nationwide |
| Device | CLASS II | ND: YAG Laser applicator for Ellipse Multiflex Medical recalled | Ellipse A/S | 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.