NA 04.137.004SRecalls & reported problems
Synthes GmbH · 2.7 VA LCKNG ANT PATELLA PL TI/3-HOLE/STERILE · 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 10886982280770), received between Jul 30, 2025 and Jul 30, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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.
Reports received per month
Most reported problems
Device problems
- Migration1
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.
InjuryJul 30, 2025Migration; Migration
IT WAS REPORTED THAT ON (B)(6) 2025, THE PATIENT UNDERWENT ORIF SURGERY FOR PATELLA FRACTURE WITH PATELLA PLATE AND SCREWS. ON (B)(6) 2025, IT WAS CONFIRMED THAT THE BONE ABOVE THE PATELLA HAD COLLAPSED. THE SALES REP URGENTLY ARRANGED FOR IMPLANTS, AND THE REVISION SURGERY WAS PERFORMED. THE SURGEON REMOVED THE THREE LAUNCH SCREWS AND THE SCREW IN THE RUPTURED AREA, REPOSITIONED THE PLATE IN PLACE, INSERTED THE SCREWS AGAIN, AND ADDED SUTURE WIRING TO COMPLETE THE PROCEDURE. THE SURGERY WAS COMPLETED SUCCESSFULLY WITHOUT ANY SURGICAL DELAY. NO FURTHER INFORMATION IS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22669508 ↗
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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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