VA-LCP 02.115.751SRecalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10886982035578), received between May 21, 2021 and Oct 4, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

Recent adverse event reports

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

• MalfunctionOct 4, 2022Material Deformation; Material Deformation

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, A TRAY FELL ON TWO STERILE BOXED IMPLANTS AND MAY HAVE BENT THE PLATES INSIDE THE BOX. THERE WAS NO PATIENT INVOLVEMENT. THIS REPORT INVOLVES ONE 2.4MM VA-LCP VOLAR RIM DISTAL RAD PL/6H HD/5H SHFT/LT-STER. THIS IS REPORT 1 OF 2 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15537171 ↗
• MalfunctionMay 21, 2021Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE 2.4 VA VOLAR RIM PLATE WAS USED AND THERE WERE TWO OF THE LOCKING HOLES THAT WOULD NOT ENGAGE WITH THE SCREWS. MULTIPLE UNKNOWN SCREWS WERE ATTEMPTED BUT DID NOT WORK. THIS REPORT IS FOR ONE (1) 2.4MM VA-LCP VOLAR RIM DISTAL RAD PL/6H HD/5H SHFT/LT-STER. THIS IS REPORT 1 OF 3 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11865595 ↗