Stryker Corporation
2,640 devices · 40,947 adverse event reports · 78 deaths reported · 220 devices named in recalls
Counts reflect reports that name each device's exact identifier. Larger companies sell more devices, so totals should not be read as a safety ranking.
- AlphaVent 3910947020Fastener, fixation, nondegradable, soft tissue1 report
- AlphaVent 3910947120Fastener, fixation, nondegradable, soft tissue1 report
- AlphaVent 3910947021Fastener, fixation, nondegradable, soft tissue1 report
- AlphaVent 3910947131Fastener, fixation, nondegradable, soft tissue1 report
- Power-PRO 2, High Configuration - No WIFI 650705550003STRETCHER, WHEELED1 report
- SPY 0502938010Laparoscope, general & plastic surgery1 report
- Target Tetra TG5414080Device, Vascular, for Promoting Embolization1 report
- 1788 1788210080Microscope, surgical1 report
- Surpass Elite FDSE32525Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE40015Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE40020Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE45017Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE45030Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE50017Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE50030Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE52525Intracranial aneurysm flow diverter1 report
- Surpass Elite FDSE52540Intracranial aneurysm flow diverter1 report
- OptaBlate 9700811000spinal channeling instrument, vertebroplasty1 report
- N/A 5502120486Orthopedic stereotaxic instrument1 report
- N/A 5502120490Orthopedic stereotaxic instrument1 report
- C2C 4607-149-032INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- Prime Series 1125Stretcher, wheeled, powered1 report
- Prime Series 1105STRETCHER, WHEELED1 report
- SurgiCount 0894000003Counter, sponge, surgical1 report
- N/A 0894000004Image processing device for estimation of external blood loss1 report
- ThermaClear 502500001Insufflator, hysteroscopic1 report
- PhotonBlade 0730101000Electrosurgical, cutting & coagulation & accessories1 report
- Iconix 3910500580Accessories, arthroscopic1 report
- Omnicurve 1032015000Arthroscope1 report
- Omnicurve 1032020000Arthroscope1 report
- Surpass Elite FDSE42512Intracranial aneurysm flow diverter1 report
- mild Device Kit MDK-0001Arthroscope1 report
- NA 234-030-027ACCESSORIES,ARTHROSCOPIC1 report
- SURGICOUNT 0632022120Gauze/sponge, internal, x-ray detectable1 report
- SURGICOUNT 0632284160GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE1 report
- SURGICOUNT 0632344160GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE1 report
- SURGICOUNT 0631004180GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE1 report
- SURGICOUNT 0694002010Counter, sponge, surgical1 report
- SURGICOUNT 0621108360GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE1 report
- SURGICOUNT 0621118180GAUZE/SPONGE, INTERNAL, X-RAY DETECTABLE1 report