Warsaw Orthopedics
FDA adverse event reports naming Warsaw Orthopedics as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: WARSAW ORTHOPEDICS.
- Total reports
- 3,710
- Deaths
- 8
- Injuries
- 1,783
- Malfunctions
- 1,902
Reports per year
6211
20912
26913
30214
31915
39516
38917
34618
29719
30620
22721
16122
14223
14024
12525
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Appliance, Fixation, Spinal InterlaminalKWP1,857
- Thoracolumbosacral Pedicle Screw SystemNKB437
- Intervertebral Fusion Device With Bone Graft, LumbarMAX434
- Prosthesis, Intervertebral DiscMJO343
- Appliance, Fixation, Spinal Intervertebral BodyKWQ294
- Orthopedic Manual Surgical InstrumentLXH62
- Dispenser, CementKIH42
- Orthosis, Spine, Plate, Laminoplasty, MetalNQW33
- Bit, DrillHTW30
- Orthosis, Spinal Pedicle FixationMNI24
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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