PRODUCT CODE FTM
Mesh, Surgical
2026-06-03 – 2026-08-31 · FDA release 2026-09-29
Monitor reported device problems. This is a lead for evidence review. A report does not establish causation, fault, an eligible claimant or a future lawsuit. Multiple devices may appear in a report; device counts cannot be added into a unique-patient total.
Reports · 90 days
77Prior 90 days: 23Injury reports
67Source-classified event typeDeath reports
1Reported relationship is unverifiedReporting change
—Prior baseline too small for percentageMalfunction-classified reports in this window: 2. These are separate from injury/death classifications.
Recent source reports
Up to five example reports. Statistics above cover all matching API-index entries in the stated windows; these examples are not a representative sample.
Large Curved Shape for Strattice, BPS (Contour3)
Read FDA report 50521461 ↗Received 2026-08-31 · Injury
Patient problems: No Clinical Signs, Symptoms or Conditions
Device problems: Lack of Effect
Large Curved Shape for Strattice, BPS (Contour3)
Read FDA report 50522686 ↗Received 2026-08-31 · Injury
Patient problems: No Clinical Signs, Symptoms or Conditions
Device problems: Lack of Effect
Surgimend matrix - unspecified
Read FDA report 50498967 ↗Received 2026-08-28 · Malfunction
Patient problems: Wound Dehiscence
Device problems: Insufficient Device Problem Information
Gynecare Mesh Unknown
Read FDA report 50508948 ↗Received 2026-08-28 · Injury
Patient problems: Bladder Dysfunction
Device problems: Adverse Event Without Identified Device or Use Problem
XenMatrix
Read FDA report 50436579 ↗Received 2026-08-25 · Injury
Patient problems: Adhesion(s); Hernia; Obstruction/Occlusion
Device problems: Material Deformation
Investigate before assessing a potential case
Review the complete report, model and device identifiers, recalls, medical literature, alternative causes and current court records. Check follow-ups and duplicate submissions. Report volume alone cannot establish incidence, liability or case value.