Aribex recalls
Aribex has 2 recalls on record with the FDA and USDA, the earliest in 2016 and the latest reported on 14 Sep 2016. The most frequent reason is packaging defects.
Total recalls2since 2016
Last 12 months0reported
Class I00% of total
Ongoing0latest 14 Sep 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 aribex is recalled
Product types
By year
All aribex recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Nomad Pro2 Packaged X-Ray System recalled by Aribex | Aribex | Packaging Defects | 50 states |
| Device | CLASS II | Nomad Pro Packaged X-Ray System recalled by Aribex | Aribex | Packaging Defects | 50 states |
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.