Arthrex® AR-9560-24SRecalls & reported problems
Arthrex, Inc. · 24mm Baseplate, MONOBLOCK SCREW · Class 2 · Implant
Data updated Oct 18, 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 00888867296442), received between Apr 17, 2024 and Apr 24, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fitting 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
- Fitting Problem1
- Unintended Movement1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 24, 2024Fitting Problem; Fitting Problem
IT WAS REPORTED ON 12/30/2022 BY A SALES REPRESENTATIVE VIA EMAIL THAT AN AR-9560-24S MODULAR BASEPLATE WOULD NOT SEAT WITH THE 15MM SCREW, SURGEON OPTED TO USE THE 25MM SCREW AND WAS ABLE TO SEAT THE BASEPLATE TO THEIR SATISFACTION. CASE INVOLVEMENT, NO PATIENT EFFECT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19175077 ↗MalfunctionApr 17, 2024Unintended Movement; Unintended Movement
ON 03/22/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA PHONE THAT AN AR-9560-24S MODULAR GLENOID SYSTEM MONOBLOCK SCREW BASEPLATE DID NOT SLIDE ON THE GLENOID PIN. IT APPEARS THE SCREW WAS NOT CENTERED, AND IT WAS WOBBLING, NOT ALLOWING IT TO SEAT CORRECTLY. THE CASE WAS COMPLETED USING A NEW AR-9560-24S MODULAR GLENOID SYSTEM MONOBLOCK SCREW BASEPLATE. THIS WAS DISCOVERED DURING AN RTS PROCEDURE ON (B)(6) 2024.
Patient problems: Insufficient Information
MAUDE report 19129613 ↗
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- 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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