DJO SURGICAL 504-50-022Recalls & reported problems
Encore Medical, L.P. · HEAD, HUMERAL W/OFFSET FEMALE TAPER, 50X22 O/S · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888912143738), received between Jun 21, 2017 and Apr 22, 2021 — classified as 2 injuries.
The most frequently reported specific device problem is “Naturally Worn” (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 18, 2026.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Naturally Worn1
Patient problems
- Pain2
- Failure of Implant1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryApr 22, 2021Appropriate Device Problem Term/Code Not Available
REVISION SURGERY - DUE TO EVENTUAL PAIN. OUR IMPLANTS WERE REMOVED AND DISPOSED OF AND REPLACED WITH A COMPETITOR IMPLANT WHICH WAS TORNIER.
Patient problems: Pain
MAUDE report 11711567 ↗InjuryJun 21, 2017Naturally Worn
REVISION SURGERY - DUE TO THE PATIENT HAVING SOME PAIN THAT HAD DEVELOPED OVER TIME. X-RAYS SHOWED LESS BONE AT THE PROXIMAL HUMERUS. IN REVISION TODAY HIS GLENOID WAS WORN MOST OF THE WAY THROUGH AND BONE AT PROXIMAL HUMOROUS WAS INSUFFICIENT AND WEAK. THE SURGEON SAID POTENTIALLY DUE TO LYSIS FROM THE EXTENSIVE POLY WEAR. IT WAS SENT TO BE WASHED IN HOPES OF BEING ABLE TO RETURN IT TO DJO FOR ANALYSIS.
Patient problems: Failure of Implant; Pain
MAUDE report 6657852 ↗
Other Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented devices
- DJO SURGICAL 508-32-204Encore Medical, L.P. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall544 reports
- Comprehensive Reverse Shoulder 010000589Biomet Orthopedics, LLC · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED1 recall142 reports
- DELTA XTEND 130738203Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED175 reports
- DJO SURGICAL 509-00-432Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented1 recall117 reports
- Alliance® SBGL3007Zimmer, Inc. · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED162 reports
- DELTA XTEND 130760138Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED146 reports
- DELTA XTEND 130790030Depuy (Ireland) · PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED132 reports
- DJO SURGICAL 509-00-436Encore Medical, L.P. · Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented124 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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