Arthrocare Corp.
FDA adverse event reports naming Arthrocare Corp. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ARTHROCARE CORP..
- Total reports
- 5,763
- Deaths
- 10
- Injuries
- 1,790
- Malfunctions
- 3,449
Reports per year
10210
30911
5012
113
614
10915
35516
44317
55918
62819
1,17720
1,05621
48222
123
126
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI3,874
- Fastener, Fixation, Nondegradable, Soft TissueMBI679
- Accessories, ArthroscopicNBH264
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT210
- PasserHWQ196
- Screw, Fixation, BoneHWC122
- Splint, Intranasal SeptalLYA78
- Orthopedic Manual Surgical InstrumentLXH77
- ArthroscopeHRX72
- Product code KOGKOG33
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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