Arthrex® AR-9507RGDP-1Recalls & reported problems
Arthrex, Inc. · Uni Revers Humeral Resection Slide Block · Class 1
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 00888867266001), received between May 1, 2019 and Mar 20, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Corroded” (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
- Corroded1
- Difficult to Advance1
- Material Protrusion/Extrusion1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 20, 2024Corroded; Corroded
IT WAS REPORTED THAT THE UNI REVERS HUMERAL RESECTION SLIDE BLOCK HAS A RUSTY SCREW. IT WAS NOTICED AFTER THE SURGERY. THERE WAS NO HARM FOR PATIENT, OPERATOR OR THIRD PARTY. THERE WAS NO CASE INVOLVEMENT REPORTED. NO FURTHER INFORMATION RECEIVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18942451 ↗InjuryMay 1, 2019Difficult to Advance; Material Protrusion/Extrusion
IT WAS REPORTED THAT DURING A REVERSE TOTAL SHOULDER ARTHROPLASTY IN THE LEFT SHOULDER, THE CUTTING BLOCK WITH BOOM WAS UNABLE TO ADVANCE TOWARDS THE PATIENT'S SHOULDER. THE SURGEON PERFORMED A FREE HANDED HUMERAL HEAD CUT AND WENT ON WITH THE CASE AS USUAL. IT WAS ALSO REPORTED THAT UPON FURTHER INSPECTION OF THE DEVICE, THERE IS A VERY SMALL SCREW NEAR THE ENTRANCE FOR THE BOOM THAT IS PROTRUDING INTO THE AREA THAT CONTACTS THE BOOM.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8569804 ↗
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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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