AESDEX recalls
AESDEX has 2 recalls on record with the FDA and USDA, the earliest in 2018 and the latest reported on 25 Jul 2018. The most frequent reason is foreign material.
Total recalls2since 2018
Last 12 months0reported
Class I00% of total
Ongoing0latest 25 Jul 2018
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 aesdex is recalled
Product types
By year
All aesdex recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Cardica C-Port xA PLUS Anastomosis System recalled by AESDEX | AESDEX | Foreign Material | Nationwide |
| Device | CLASS II | Cardica C-Port Flex-A PLUS Distal Anastomosis System recalled by AESDEX | AESDEX | Foreign Material | 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.