Arthrex® AR-1920S-1Recalls & reported problems
Arthrex, Inc. · SUTR ANCH,CRKSCRW · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888867022812), received between Jun 9, 2017 and Jun 9, 2017 — classified as 1 injury.
The most frequently reported specific device problem is “Torn Material” (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.
Most reported problems
Device problems
- Torn Material1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 9, 2017Torn Material
IT WAS REPORTED THAT THE SUTURE ANCHOR WAS IMPLANTED ON THE (B)(6) 2017 AND REMOVED ON THE (B)(6) 2017 BECAUSE THE SUTURE WAS TORN OFF. FOLLOW-UP ON (B)(6) 2017: THE INCIDENT CAUSED NO HARM FOR THE PATIENT AND NO CONSEQUENTIAL DAMAGES APPEARED. THEY USED ANOTHER (B)(4) WITH A DIFFERENT LOT NUMBER IN THE SECOND SURGERY. THE SURGEON REPORTED THAT HE COULD TEAR THE SUTURE WITH HIS HANDS.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6630317 ↗
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- PRECICE® Bone Transport System STP3.5-350Nuvasive 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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