Boston Scientific - Spencer
FDA adverse event reports naming Boston Scientific - Spencer as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC - SPENCER.
- Total reports
- 11,000
- Deaths
- 51
- Injuries
- 2,938
- Malfunctions
- 8,007
Reports per year
206
108
1809
1,64910
1,50711
1,36112
1,35413
1,02114
1,20015
1,08416
91517
88818
Source: FDA adverse event reports by year received, 2006–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Tubes, Gastrointestinal (And Accessories)KNT1,781
- Stents, Drains And Dilators For The Biliary DuctsFGE1,344
- Ligator, HemorrhoidalFHN1,047
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS972
- Lithotriptor, Biliary MechanicalLQC712
- Choledochoscope And Accessories, Flexible/RigidFBN692
- Dislodger, Stone, Basket, Ureteral, MetalFFL557
- Mesh, Surgical, PolymericFTL467
- Ligator, EsophagealMND455
- Electrosurgical, Cutting & Coagulation & AccessoriesGEI402
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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