Arthrex® AR-1927PSF-65Recalls & reported problems
Arthrex, Inc. · SUTURE ANCHOR, PEEK CORKSCREW FT · Class 2 · Implant
Data updated Oct 16, 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 00888867023673), received between Aug 26, 2024 and Aug 26, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Defective Device” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Defective Device1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 26, 2024Defective Device; Defective Device
ON 7/18/2024, IT WAS REPORTED BY A SALES REPRESENTATIVE VIA EMAIL THAT AN AR-1927PSF-65 PEEK CORKSCREW FT ANCHOR WAS DEFECTIVE. THE SURGEON NOTICED THIS DURING THE INSERTION OF THE ANCHOR. THE CASE WAS COMPLETED USING ANOTHER AR-1927PSF-65 PEEK CORKSCREW FT. THIS WAS DISCOVERED DURING AN RCR PROCEDURE ON (B)(6) 2024. ADDITIONAL INFORMATION RECEIVED ON 7/30/2029: THE ANCHOR TIP WAS ALTERED AFTER AN ATTEMPT TO INSERT THE ANCHOR INTO BONE. NO PIECES OF THE ANCHOR BROKE OFF. THE CASE WAS NOT DELAYED, AND ADDITIONAL ANESTHESIA WAS NOT NEEDED.
Patient problems: Insufficient Information
MAUDE report 20063563 ↗
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- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
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- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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