Mini-Open Latarjet 71935462Recalls & reported problems
Smith & Nephew, Inc. · GLENOID DRILL GUIDE LONG BULLET · Class 1
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 00885556660003), received between Jun 8, 2021 and Jun 8, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Material Deformation” (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 Deformation1
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.
InjuryJun 8, 2021Material Deformation; Material Deformation
IT WAS REPORTED THAT, DURING A ACL SURGERY WHILE THE INSTRUMENT WAS INSIDE OF THE PATIENT, THE TIP OF THE GLENOID DRILL GUIDE LONG BULLET IS FLARED, CAUSING IT TO CATCH ON SOFT TISSUE AND NOT GO IN STRAIGHT AND CORRECT. THE SURGEON HAD TO REDRILL, WHICH MADE A LARGER HOLE AND CANNULATED DRILL WAS NOT AS SECURE IN POSITION. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITHOUT DELAY USING THE SAME DEVICE. NO PATIENT INJURY OR OTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11962752 ↗
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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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