Vilex AVID Plate AMP53-10LRecalls & reported problems
Vilex LLC · Plate, AVID MTP Large 10° L Lkng · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841731115942), received between Feb 6, 2021 and Jan 13, 2023 — classified as 2 malfunctions.
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 18, 2026.
Most reported problems
Device problems
- Fracture1
- No Apparent Adverse Event1
Patient problems
- Failure of Implant1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 13, 2023Fracture; Fracture
ISSUE INVOLVING AN IMPLANT INSERTER INSTRUMENT. TOWARDS THE END OF THE SURGERY AND THE IMPLANT WAS FULLY SEATED, A PIN FROM THE INSERTER INSTRUMENT BROKE IN THE IMPLANT. THE PIECE WAS FLUSH WITH THE IMPLANT WITH NO PROTRUSIONS AND THE SURGEON DECIDED TO COMPLETE THE SURGERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16159715 ↗MalfunctionFeb 6, 2021No Apparent Adverse Event; No Apparent Adverse Event
DURING POST-OP VISIT IT WAS DETEREMINED THAT THE AVID PLATE HAD BROKEN.
Patient problems: Failure of Implant
MAUDE report 11290271 ↗
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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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