AccuMesh AMPMEDRecalls & reported problems
Covidien LP · Articulating Mesh Positioning Device with Medium Frame · Class 2 · Implant
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521171282), received between Sep 2, 2019 and Dec 6, 2019 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Loss of or Failure to Bond” (2 reports).
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.
Most reported problems
Device problems
- Loss of or Failure to Bond2
Patient problems
- No Consequences Or Impact To Patient2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 6, 2019Loss of or Failure to Bond; Loss of or Failure to Bond
ACCORDING TO THE REPORTER, ACCUMESH POSITIONING DEVICE FOR MESH SEEMED TO FAIL. NO HARM TO PATIENT. A REPLACEMENT DEVICE USED. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9432461 ↗MalfunctionSep 2, 2019Loss of or Failure to Bond; Loss of or Failure to Bond
ACCORDING TO THE REPORTER, DURING LAPAROSCOPIC VENTRAL HERNIA PROCEDURE, WHILE ON ABDOMINAL CAVITY, THE MESH BUNCHED UP WHEN TRYING TO DEPLOY AND THE ARM BENT AND WOULD NOT EXPAND. THE SURGEON ENDED UP USING STAY SUTURES TO FLAT, POSITIONED AND ATTACH THE MESH. SURGICAL TIME WAS EXTENDED FOR 30 MINUTES. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 8953352 ↗
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 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
- 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page