RESILIENCE™ A (REF RE206)Recalls & reported problems
Merit Medical Systems, Inc. · Class 2 · Implant
- Adverse event reports
- 2
- Deaths reported
- 1
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00884450094105), received between Jul 1, 2026 and Sep 30, 2026 — classified as 1 death, 1 injury.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Detachment of Device or Device Component1
- Device Dislodged or Dislocated1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Perforation1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
DeathSep 30, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Perforation
MAUDE report 50947123 ↗InjuryJul 1, 2026Detachment of Device or Device Component; Device Dislodged or Dislocated
CUSTOMER REPORTS WHILE DEPLOYING AN ESOPHAGEAL STENT, THE STENT SLIPPED OUT OF THE DEVICE AND MIGRATED TO THE PATIENT'S STOMACH. THE PROCEDURE WAS CANCELLED AND THE PATIENT REMAINS IN THE HOSPITAL FOR ANOTHER DAY FOR A NEW STENT PLACEMENT AND RETRIEVAL ATTEMPT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25680658 ↗
Other PROSTHESIS, ESOPHAGEAL devices
- WallFlex™ Esophageal M00516730Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall29 reports
- WallFlex™ Esophageal M00516740Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall1 death22 reports
- WallFlex™ Esophageal M00516750Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall1 death19 reports
- WallFlex™ Esophageal M00516700Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall18 reports
- WallFlex™ Esophageal M00516910Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall15 reports
- WallFlex™ Esophageal M00516930Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall14 reports
- WallFlex™ Esophageal M00516710Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall13 reports
- WallFlex™ Esophageal M00516940Boston Scientific Corporation · PROSTHESIS, ESOPHAGEAL1 recall12 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.