Pioneer Surgical Technology recalls
Pioneer Surgical Technology has 3 recalls on record with the FDA and USDA, the earliest in 2014 and the latest reported on 17 Sep 2014. The most frequent reason is sterility.
Total recalls3since 2014
Last 12 months0reported
Class I00% of total
Ongoing0latest 17 Sep 2014
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 pioneer surgical technology is recalled
Product types
By year
All pioneer surgical technology recalls, newest first
3 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Streamline MIS Spinal Fixation System Fixed Rod Holder NON Sterile recalled | Pioneer Surgical Technology | Sterility | Nationwide |
| Device | CLASS II | Streamline CT Cervico-thoracic System recalled | Pioneer Surgical Technology | Sterility | 7 states |
| Device | CLASS II | Tritium Sternal Plate System, Screw, Sterile recalled | Pioneer Surgical Technology | 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.