BioHorizons Implant Systems recalls
BioHorizons Implant Systems has 5 recalls on record with the FDA and USDA, the earliest in 2012 and the latest reported on 16 Dec 2015. The most frequent reason is sterility.
Total recalls5since 2012
Last 12 months0reported
Class I00% of total
Ongoing0latest 16 Dec 2015
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 5 100%Class III 0 0%
Why biohorizons implant systems is recalled
Product types
By year
All biohorizons implant systems recalls, newest first
5 total| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | RBT, Internal Implant, Laser-Lok, 0, 7 Platform recalled | BioHorizons Implant Systems | Labeling Errors | Nationwide |
| Device | CLASS II | Tapered HD Upgrade Set recalled by BioHorizons Implant Systems | BioHorizons Implant Systems | Foreign Material | Nationwide |
| Device | CLASS II | External Implant RBT, D3 Threadform recalled | BioHorizons Implant Systems | Sterility | Nationwide |
| Device | CLASS II | Titanium Tack Starter Kit recalled by BioHorizons Implant Systems | BioHorizons Implant Systems | Sterility | Nationwide |
| Device | CLASS II | AutoTac Delivery Handle recalled by BioHorizons Implant Systems | BioHorizons Implant Systems | 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.