TARGETRecalls & reported problems across all models
Stryker Corporation · 114 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
TARGET models — page 2
114 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- TARGET M0035452020DEVICE, NEUROVASCULAR EMBOLIZATION2 reports
- Target M0035433040Device, Vascular, for Promoting Embolization1 report
- TARGET M0035464100DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- TARGET M0035468300DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- TARGET M0035476100Device, Vascular, for Promoting Embolization1 report
- TARGET M0035431510Device, Vascular, for Promoting Embolization1 report
- Target M0035433560Device, Vascular, for Promoting Embolization1 report
- TARGET M0035463080DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- TARGET M0035467150DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- TARGET M0035471330Device, Vascular, for Promoting Embolization1 report
- TARGET M0035471430Device, Vascular, for Promoting Embolization1 report
- TARGET M0035464150DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- Target M0036153060DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- Target M0036157150DEVICE, NEUROVASCULAR EMBOLIZATION1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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