Mentor Worldwide LLC
FDA adverse event reports naming Mentor Worldwide LLC as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: MENTOR WORLDWIDE LLC.
- Total reports
- 1,766
- Deaths
- 0
- Injuries
- 1,681
- Malfunctions
- 62
Reports per year
15512
57513
18714
13715
3916
7417
718
26919
14120
5121
2222
3723
2724
1225
526
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorOTN545
- Mesh, Surgical, PolymericFTL482
- Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-FilledFTR475
- Prosthesis, Breast, Inflatable, Internal, SalineFWM210
- System, Suction, LipoplastyMUU32
- Tissue Expander And AccessoriesLCJ23
- Regulator, Pressure, Gas CylinderCAN8
- Mammary SizerMRD5
- Mesh, Surgical, For Stress Urinary Incontinence, MaleOTM5
- Mesh, SurgicalFTM2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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