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.
- AVIATOR 48814016APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- AVS AL 48326084Intervertebral fusion device with integrated fixation, lumbar1 report
- SYNCHRO 14 M00313320WIRE, GUIDE, CATHETER1 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
- Neuroform3 M003SNF340200intracranial neurovascular stent1 report
- Neuroform3 M003SNF345200intracranial neurovascular stent1 report
- TARGET M0035464150DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- AVS NAVIGATOR 48392094Intervertebral fusion device with bone graft, lumbar1 report
- AVS NAVIGATOR 48392084Intervertebral fusion device with integrated fixation, lumbar1 report
- AVS NAVIGATOR 48392104Intervertebral fusion device with integrated fixation, lumbar1 report
- AVS NAVIGATOR 48392110Intervertebral fusion device with integrated fixation, lumbar1 report
- AVS NAVIGATOR 48392114Intervertebral fusion device with bone graft, lumbar1 report
- AVS NAVIGATOR 48393110Intervertebral fusion device with integrated fixation, lumbar1 report
- AVS NAVIGATOR 48393150Intervertebral fusion device with bone graft, lumbar1 report
- AVIATOR 48834514APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- AVIATOR 48834518APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- AVIATOR 48844018APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 48235480Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ICONIX 3910-500-569BIT, DRILL1 report
- ICONIX 3910-500-571BIT, DRILL1 report
- OASYS 48553608APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- AVS Anchor-L 48662102Intervertebral fusion device with bone graft, lumbar1 report
- AVS Anchor-L 48662104Intervertebral fusion device with integrated fixation, lumbar1 report
- AVS Anchor-L 48662128Intervertebral fusion device with bone graft, lumbar1 report
- AVS Anchor-L 48662142Intervertebral fusion device with integrated fixation, lumbar1 report
- AVS Anchor-L 48663122Intervertebral fusion device with bone graft, lumbar1 report
- AVS Anchor-L 48663128Intervertebral fusion device with bone graft, lumbar1 report
- AVS Anchor-L 48665025Intervertebral fusion device with bone graft, lumbar1 report
- AVS Anchor-L 48992001Intervertebral fusion device with bone graft, lumbar1 report
- TransPort CAT00223ACCESSORIES,ARTHROSCOPIC1 report
- FlowPort CAT00777Accessories, arthroscopic1 report
- CinchLock CAT02463BIT, DRILL1 report
- Surpass Streamline M003SFD030250Intracranial aneurysm flow diverter1 report
- Surpass Streamline M003SFD040400Intracranial aneurysm flow diverter1 report
- Surpass Streamline M003SFD050500Intracranial aneurysm flow diverter1 report
- Neuroform Atlas M003SZAS45210intracranial neurovascular stent1 report
- Stryker Performance Series 6213147070INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- XIA 3 482378560APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 482378580Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- XIA 3 482397012ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482807060ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482807065Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482807080Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482806050Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482806070Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482807480Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482806090ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482807180Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482802425ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482802440Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482802530APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482802545Orthosis, spinal pedicle fixation, for degenerative disc disease1 report
- ES2 SPINAL SYSTEM 482802550APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482802655Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482802755Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804540Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804640ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482804735APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482804435Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804790APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 482804855Orthosis, spondylolisthesis spinal fixation1 report
- ES2 SPINAL SYSTEM 482804870ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- ES2 SPINAL SYSTEM 482804890ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 3 482377590Orthosis, spondylolisthesis spinal fixation1 report
- XIA 3 482378570APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY1 report
- XIA 3 482377580Orthosis, spondylolisthesis spinal fixation1 report
- XIA 4 5 481321060APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- XIA 4 5 481322050ORTHOSIS, SPINAL PEDICLE FIXATION1 report
- XIA 4 5 481322060APPLIANCE, FIXATION, SPINAL INTERLAMINAL1 report
- ES2 SPINAL SYSTEM 48280175ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- POWEReam 4405260000INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT1 report
- TRANSFORM M003SRC03150Catheter, intravascular occluding, temporary1 report
- TRANSFORM M003SRC04150Catheter, intravascular occluding, temporary1 report
- TARGET XL M0036102250Device, Vascular, for Promoting Embolization1 report
- TARGET XL M0036108300Device, Vascular, for Promoting Embolization1 report
- TARGET XL M0036109300DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- Target M0036153060DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- Target M0036157150DEVICE, NEUROVASCULAR EMBOLIZATION1 report
- ES2 SPINAL SYSTEM 48280090ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- DYNATRAN 48515021ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- AVS Anchor-C Cervical Cage System 48328808ORTHOPEDIC MANUAL SURGICAL INSTRUMENT1 report
- NA 0225426000WAPPARATUS, AUTOTRANSFUSION1 report
- NA 0233050065Light source, fiberoptic, routine1 report
- NA 0233050084Light source, fiberoptic, routine1 report
- NA 0233065010Light source, fiberoptic, routine1 report
- Strykeprobe 0250070450Laparoscope, general & plastic surgery1 report
- Strykeprobe 0250070453ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 report
- NA 0250080234Endoscopic grasping/cutting instrument, non-powered1 report
- NA 0250080260Endoscopic grasping/cutting instrument, non-powered1 report
- NA 0295723100Accessories, arthroscopic1 report
- NA 0295725100Accessories, arthroscopic1 report
- Conquest Series 0300034702Accessories, arthroscopic1 report
- Conquest Series 0300034703Accessories, arthroscopic1 report
- Speed-Lock 0502244030ARTHROSCOPE1 report
- Speed-Lock 0747031510Accessories, arthroscopic1 report
- Speed-Lock 0747031530TRAY, SURGICAL, INSTRUMENT1 report
- Formula 0375940000BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL1 report