Xintec recalls
Xintec has 2 recalls on record with the FDA and USDA, the earliest in 2017 and the latest reported on 30 Oct 2019. The most frequent reason is sterility.
Total recalls2since 2017
Last 12 months0reported
Class I00% of total
Ongoing0latest 30 Oct 2019
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 1 50%Class III 1 50%
Why xintec is recalled
Product types
By year
All xintec recalls, newest first
2 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS III | OptiLITE, Products for Laser Surgery recalled by Xintec | Xintec | Sterility | PA, VA |
| Device | CLASS II | OptiLITE(TM) Products for Laser Surgery recalled by Xintec | Xintec | Sterility | 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.