Arthrex® AR-7202-1Recalls & reported problems
Arthrex, Inc. · FW BPB #2 SUTR,BLU W/NDL · Class 2 · Implant
Data updated Oct 16, 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 00888867279131), received between Aug 1, 2022 and Aug 1, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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.
Most reported problems
Device problems
- Material Split, Cut or Torn1
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.
InjuryAug 1, 2022Material Split, Cut or Torn
IT WAS REPORTED THAT A PATIENT WHO WAS TREATED WITH THE FIBERWIRE DEVICE TWO WEEKS BEFORE THE (B)(6) 2022 NEEDED A REVISION SURGERY FOR OTHER REASONS. DURING THE REVISION SURGERY ON THE (B)(6) 2022 THE SURGEON NOTICED THAT THE FIBERWIRE SUTURE HAD TORN. NO FURTHER INFORMATION RECEIVED. UPDATE (B)(6) 2022: IT WAS CONFIRMED THAT THE TORN SUTURES OF THE DEVICE WERE NOT THE REASON FOR THE REVISION.
Patient problems: Insufficient Information
MAUDE report 15137910 ↗
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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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