Arthrex® AR-8933V-22SRecalls & reported problems
Arthrex, Inc. · 3.0 X 22MM VAL SCREW, TI, STRL · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867210301), received between Jul 16, 2025 and Jul 16, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Fragmentation” (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
- Material Fragmentation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 16, 2025Material Fragmentation; Material Fragmentation
ON 6/19/2025, IT WAS REPORTED VIA EMAIL BY AN ARTHREX SUBSIDIARY EMPLOYEE THAT DURING A PROCEDURE ON (B)(6) 2025 INVOLVING AN AR-8933V-22S LOW PROFILE VA LOCKING SCREW, A PIECE OF METAL WAS OBSERVED DISLODGING UPON SCREW INSERTION. THE SCREW WAS REMOVED AND REINSERTED, AND THE PROCEDURE WAS SUCCESSFULLY COMPLETED. ALL DEBRIS WAS RETRIEVED, AND NO PATIENT HARM WAS REPORTED. ADDITIONAL INFORMATION WAS REQUESTED ON 07/03/2025: THIS OCCURRED DURING A HALLUX VALGUS PROCEDURE ON (B)(6) 2025. THE CASE WAS COMPLETED BY USING THE INITIAL SCREW BY REMOVING IT ONCE AND THEN REINSERTING IT TO COMPLETE THE SURGERY. NO CASE DELAY OR ADDED ANESTHESIA WAS ADMINISTERED TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22520964 ↗
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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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