Tissue Science Laboratories
FDA adverse event reports naming Tissue Science Laboratories as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: TISSUE SCIENCE LABORATORIES.
- Total reports
- 2,294
- Deaths
- 5
- Injuries
- 2,262
- Malfunctions
- 9
Reports per year
4011
31012
1,19813
1214
1015
216
15317
12718
20719
10020
4021
1022
1423
1624
525
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
- Mesh, SurgicalFTM1,162
- Mesh, Surgical, PolymericFTL1,067
- Mesh, Surgical, Non-Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorPAG40
- Mesh, Surgical, Non-Synthetic, Urogynecologic, For Pelvic Organ Prolapse, Transvaginally PlacedPAI22
- Staple, ImplantableGDW1
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or TransobturatorOTN1
- Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-SlingPAH1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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