Arthrex® AR-9580-2420SRecalls & reported problems
Arthrex, Inc. · 24MM BASEPLATE, 20° FULL AUG, ST · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00888867352063), received between Aug 5, 2024 and Sep 19, 2025 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Patient Device Interaction Problem” (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.
Reports received per month
Most reported problems
Device problems
- Patient Device Interaction Problem1
- Positioning Failure1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- Pain1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 19, 2025Positioning Failure; Positioning Failure
ON 08/29/2025, A SALES REPRESENTATIVE REPORTED VIA EMAIL THAT AN AR-9580-2420S UNIVERS REVERS MODULAR GLENOID SYSTEM AUGMENTED BASE PLATE (24 MM) AND THE AR-9675-S ANGLED REAMER DID NOT FUNCTION PROPERLY DURING A PROCEDURE. THE PATIENT WAS NOT IMPACTED, AS REPLACEMENT DEVICES OF THE SAME MODELS WERE USED SUCCESSFULLY. THIS WAS DISCOVERED DURING A PROCEDURE ON (B)(6) 2025, WITH NO REPORTED PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN REQUESTED ON 09/05/2025.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23098837 ↗InjuryAug 5, 2024Patient Device Interaction Problem; Patient Device Interaction Problem
ADDITIONAL INFORMATION RECEIVED ON 11/4/2024: ON (B)(6) 2024, THE PATIENT'S IMPLANTS WERE CONVERTED FROM FAILED REVERS TO A HEMIARTHROPLASTY DUE TO THE DISPLACED GLENOID COMPONENTS FROM THE BROKEN SCREWS. AT THIS TIME, IT IS UNKNOWN WHICH ARTHREX PRODUCTS FROM THE ORIGINAL SURGERY ON (B)(6) 2023 WERE EXPLANTED DURING THE REVISION SURGERY ON (B)(6) 2024.
Patient problems: Pain
MAUDE report 19907112 ↗
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- DJO SURGICAL 508-32-104Encore Medical, L.P. · shoulder prosthesis, reverse configuration1 recall203 reports
- DJO SURGICAL 509-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration233 reports
- DELTA XTEND 130760000Depuy (Ireland) · shoulder prosthesis, reverse configuration223 reports
- DJO SURGICAL 508-00-032Encore Medical, L.P. · shoulder prosthesis, reverse configuration122 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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