SUTURE CROCHET HOOK 903610Recalls & reported problems
Biomet Orthopedics, LLC · Class 1
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 00880304404939), received between Sep 21, 2020 and Sep 21, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
Patient problems
- No Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 21, 2020Fracture; Fracture
IT WAS REPORTED DURING THE INSPECTION OF THE KIT THE TIP OF THE PRODUCT WAS DISCOVERED AS FRACTURED. IT IS UNKNOWN WHEN THE BREAK OCCURRED. ATTEMPTS HAVE BEEN MADE AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Patient problems: No Patient Involvement
MAUDE report 10560923 ↗
Other HOOK, SURGICAL, GENERAL & PLASTIC SURGERY devices
- NICO BrainPath NN-8026Nico Corporation · Hook, Surgical, General & Plastic Surgery1 recall0 reports
- NICO BrainPath NN-8024Nico Corporation · Hook, Surgical, General & Plastic Surgery1 recall0 reports
- Centurion I68785Centurion Medical Products Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- Sklar Instruments 96-4022MSklar Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- NICO BrainPath NN-8025Nico Corporation · Hook, Surgical, General & Plastic Surgery1 recall0 reports
- Sklar Instruments 96-4021MSklar Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- Sklar Instruments 96-4020MSklar Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
- Centurion 67810Centurion Medical Products Corporation · HOOK, SURGICAL, GENERAL & PLASTIC SURGERY1 recall0 reports
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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