Tornier Flex Shoulder System DWH051Recalls & reported problems
Tornier · Tornier Pyrocarbon Humeral Head · Class 2 · Implant
All models of Tornier Flex Shoulder System (91)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 03700434019988), received between Feb 21, 2025 and Feb 21, 2025 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Loss of Range of Motion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
THE MANUFACTURER RECEIVED A REPORT FROM THE NATIONAL JOINT REGISTRY THAT CONTAINS UNPUBLISHED COLLECTED DATA ON THE USAGE AND THE OUTCOMES OF THE SHOULDER REPLACEMENT. THE REPORT DETAILS ANALYSIS PROVIDED FOR REVISION PROCEDURES PERFORMED UNTIL (B)(6) 2025. DURING THE REVIEW OF THE REPORT, IT WAS IDENTIFIED THAT ON (B)(6) 2024 A PATIENT REQUIRED REVISION SURGERY DUE TO STIFFNESS WHICH WAS NOT PREVIOUSLY REPORTED TO THE MANUFACTURER. REVISION PROCEDURE TYPE: REVISION STEMMED TOTAL REVERSE ARTHROPLASTY.
Patient problems: Loss of Range of Motion
MAUDE report 21433417 ↗
Other Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis devices
- Tornier Flex Shoulder System DWH146Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis6 reports
- Tornier Flex Shoulder System DWH043Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis5 reports
- Tornier Flex Shoulder System DWH046Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis5 reports
- Tornier Flex Shoulder System DWH151Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis4 reports
- Tornier Flex Shoulder System DWH139Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis3 reports
- Tornier Flex Shoulder System DWH150Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis3 reports
- Tornier Flex Shoulder System DWH143Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis2 reports
- Tornier Flex Shoulder System DWH152Tornier · Shoulder joint humeral (hemi-shoulder) ceramic head/metallic stem cemented or uncemented prosthesis2 reports
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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