VENTRALIGHT 5991525Recalls & reported problems
Davol Inc. · Ventralight ST Mesh with Echo 2 Positioning System, 6" x 10" (15 x 25 cm), Oval · Class 2 · Implant
All models of VENTRALIGHT (28)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00801741131011), received between Feb 5, 2025 and Feb 5, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Detachment of Device or Device Component1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 5, 2025Detachment of Device or Device Component; Detachment of Device or Device Component
AS REPORTED, DURING A LAPAROSCOPIC HERNIA REPAIR PROCEDURE, WHEN THE PACKAGE OF VENTRALIGHT ST W/ECHO 2 PS WAS OPENED, THE MESH WAS NOTED TO BE DAMAGED AND ¿IT FELL APART.¿ THERE WAS NO DAMAGE TO THE PACKAGING AS REPORTED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21311668 ↗
Other Mesh, surgical, deployer devices
- Bioinductive Implant with Arthroscopic Delivery System - Large 4566Smith & Nephew, Inc. · Mesh, Surgical, Deployer24 reports
- Bioinductive Implant with Arthroscopic Delivery System - Medium 4565Smith & Nephew, Inc. · Mesh, Surgical, Deployer24 reports
- VENTRALIGHT 5991520Davol Inc. · Mesh, surgical, deployer12 reports
- Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Medium 2169-2Smith & Nephew, Inc. · Mesh, Surgical, Deployer4 reports
- AccuMesh AMPMEDCovidien LP · Mesh, surgical, deployer2 reports
- Phasix 1212025Davol Inc. · Mesh, surgical, deployer1 report
- Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Large 2169-3Smith & Nephew, Inc. · Mesh, Surgical, Deployer1 report
- AccuMesh AMPPCO15XCovidien LP · Mesh, surgical, deployer1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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