VENTRALIGHT 5991823Recalls & reported problems
Davol Inc. · Ventralight ST Mesh with Echo 2 Positioning System, 7" x 9" (18 x 23 cm), Ellipse · Class 2 · Implant
- 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 00801741131028), received between Jul 17, 2024 and Jul 17, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Expiration Date Error” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Expiration Date Error1
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.
MalfunctionJul 17, 2024Expiration Date Error; Expiration Date Error
AS REPORTED, DURING A LAPAROSCOPIC INCISIONAL HERNIA REPAIR ON (B)(6) 2024, THE PATIENT WAS IMPLANTED WITH A VENTRALIGHT ST MESH W/ ECHO 2 WHICH HAD A LABELED EXPIRATION DATE OF 28-FEB-2024. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19760964 ↗
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
- AccuMesh AMPPCO2015XCovidien LP · Mesh, surgical, deployer1 report
- Phasix 1212025Davol Inc. · Mesh, surgical, deployer1 report
- Rotation Medical Reconstituted Collagen Scaffold - Arthroscopic, Large 2169-3Smith & Nephew, Inc. · Mesh, Surgical, Deployer1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.