NA 02.207.090Recalls & reported problems
Synthes GmbH · 7.3MM CANNULATED LOCKING SCREW 90MM · 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 10886982051875), received between Jan 26, 2023 and Jan 26, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Device Slipped” (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
- Device Slipped1
- Migration1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 26, 2023Device Slipped; Migration; Device Slipped; Migration
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN CANADA AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2022, A 7.3 CANNULATED LOCKING SCREW THAT HAD BEEN USED IN THE SECOND HOLE OF THE PROXIMAL END OF A PROXIMAL FEMUR LCP PLATE BECAME LOOSE AND HAS BACKED OUT. THIS WAS NOTICED BY THE PATIENT SEVERAL DAYS AFTER SURGERY WHEN THEY NOTICED SOMETHING POPPING AND CLUNKING. THE PATIENT REQUIRED HARDWARE REMOVAL OR REVISION SURGERY. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE 7.3MM CANNULATED LOCKING SCREW 90MM. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Failure of Implant
MAUDE report 16247764 ↗
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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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