Arthrosurface recalls
Arthrosurface appears in 6 official U.S. recall notices indexed by RecallRadar, most recently on 2015-12-30.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
Recall summary
| Recall notices | 6 |
|---|---|
| Published | 2015-02-18 to 2015-12-30 |
| By agency | FDA Device (6) |
| By classification | Class II (6) |
| By status | terminated (6) |
| Distribution named in notices | CA, PA, US, WV |
Recalls
- Total Toe Instrument Kit, Labeled in part: "Instrument Set, 15mm Toe, Dorsal Flange Combi" Part Number: 9000-3002 The component in question…
FDA Device · Class II · 2015-12-30 · Arthrosurface
Reason: An oversight in the implementation of the design change record resulted in outdated components being shipped to customers. The component did not pass a half-cycle sterilization. - Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component
FDA Device · Class II · 2015-02-18 · Arthrosurface
Reason: Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications. - Athrosurface 40mm 13.75x31mm Taper Post Fixation Component
FDA Device · Class II · 2015-02-18 · Arthrosurface
Reason: Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications. - Arthrosurface 25&30mm 12.5x32mm Taper Post Fixation Component
FDA Device · Class II · 2015-02-18 · Arthrosurface
Reason: Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications. - Arthrosurface HHXL (OVO) 15.6x32mm Taper Post Fixation Component
FDA Device · Class II · 2015-02-18 · Arthrosurface
Reason: Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications. - Arthrosurface 35mm 13.5x32mm Taper Post Fixation Component
FDA Device · Class II · 2015-02-18 · Arthrosurface
Reason: Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.