VA-LCP 02.127.220Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982043504), received between Mar 8, 2019 and May 6, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (2 reports).

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

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 6, 2024Device-Device Incompatibility; Material Twisted/Bent; Device-Device Incompatibility; Material Twisted/Bent

  IT WAS REPORTED THAT ON (B)(6) 2024, THE PLATE HAD A SCREW HOLE THAT WOULDN'T ALLOW A LOCKING SCREW TO LOCK IN. THE HOLE WAS STRIPPED SOMEHOW. THE PLATE HOLE LOOKED SUSPECT PRIOR TO CASE AND WAS TESTED WITH A LOCKING SCREW. THE SCREW WORKED IN OTHER HOLES, SO IT WAS DETERMINED THE SCREW WAS NOT THE ISSUE. THIS WAS DISCOVERED PRE-OPERATIVELY. THERE WAS NO PATIENT INVOLVEMENT. THIS REPORT IS FOR A PLATE. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19252894 ↗
• MalfunctionMar 8, 2019Device-Device Incompatibility; Material Twisted/Bent; Device-Device Incompatibility; Material Twisted/Bent

  IT WAS REPORTED THAT DURING AN UNKNOWN PROCEDURE ON (B)(6) 2019, THE VARIABLE ANGLE (VA) LOCKING COMPRESSION PLATE (LCP) PROXIMAL TIBIA SMALL BEND VEIN PLATE WOULD NOT CONNECT TO THE PERCUTANEOUS AIMING ARM. THE THRASHED HOLES ON THE PLATE WERE FAULTY. IT WAS RULED OUT THAT THE AIMING ARM DOES NOT HAVE ANY ALLEGATION SINCE DEVICE WAS ABLE TO HOOK UP WITH OTHER PLATES. A LCP LISS (LESS INVASIVE STABILIZATION SYSTEM) PLATE WAS USED AS A BACK-UP. PROCEDURE OUTCOME WAS GOOD. EVENT OCCURRED ON THE BACK TABLE. DEVICE NEVER ENTERED THE PATIENT. THERE WAS NO SURGICAL DELAY. THERE WAS NO NEGATIVE OUTCOME TO THE PATIENT. CONCOMITANT DEVICE REPORTED: UNK - AIMING: PERCUTANEOUS (PART # UNKNOWN, LOT # UNKNOWN, QUANTITY 1). THIS REPORT IS FOR ONE (1) 3.5MM VA-LCP PROX TIBIA PLATE. THIS IS REPORT 1 OF 1 FOR (B)(4).

  Patient problems: No Consequences Or Impact To Patient

  MAUDE report 8405389 ↗