Boston Scientific - Marlborough
FDA adverse event reports naming Boston Scientific - Marlborough as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BOSTON SCIENTIFIC - MARLBOROUGH.
- Total reports
- 25,574
- Deaths
- 43
- Injuries
- 18,901
- Malfunctions
- 6,627
Reports per year
208
3509
1,43710
1,33011
3,53712
12,54813
1,78414
1,11615
1,39416
1,48817
90318
Source: FDA adverse event reports by year received, 2008–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Mesh, Surgical, PolymericFTL14,625
- Mesh, Surgical, Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally PlacedOTP1,838
- Product code KOGKOG1,354
- Ligator, EsophagealMND1,333
- Powered Laser Surgical InstrumentGEX1,266
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorOTN999
- Mesh, Surgical, Non-Synthetic, Urogynecologic, For Apical Vaginal And Uterine Prolapse, Transabdominally PlacedPAJ681
- Hemostatic Metal Clip For The Gi TractPKL555
- Unit, Electrosurgical, Endoscopic (With Or Without Accessories)KNS532
- Device, Thermal Ablation, EndometrialMNB450
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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