Synthes Elmira
FDA adverse event reports naming Synthes Elmira as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: SYNTHES ELMIRA.
- Total reports
- 2,099
- Deaths
- 4
- Injuries
- 1,574
- Malfunctions
- 520
Reports per year
207
1908
2109
6610
14011
41312
44513
23514
24515
22516
28717
118
Source: FDA adverse event reports by year received, 2007–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Plate, Fixation, BoneHRS896
- Rod, Fixation, Intramedullary And AccessoriesHSB526
- Appliance, Fixation, Nail/Blade/Plate Combination, Multiple ComponentKTT205
- Plate, BoneJEY119
- Instrument, Surgical, Orthopedic, Ac-Powered Motor And Accessory/AttachmentHWE43
- Bit, DrillHTW34
- Thoracolumbosacral Pedicle Screw SystemNKB29
- Appliance, Fixation, Nail/Blade/Plate Combination, Single ComponentKTW26
- Screw, Fixation, BoneHWC20
- Intervertebral Fusion Device With Bone Graft, LumbarMAX20
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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