NA 02.221.101SRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10886982276032), received between Apr 21, 2025 and May 7, 2026 — classified as 1 injury, 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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 7, 2026Device-Device Incompatibility

  IT WAS REPORTED DURING A PPFX SURGERY THAT THE VA LOCKING PPFX GREATER TROCHANTER RING COULD NOT BE THREADED ONTO THE PROXIMAL FEMUR PLATE. ATTEMPTS TO ENGAGE A SECOND RING PLATE ALSO FAILED, RESULTING IN THE INABILITY TO IMPLANT ANY RING PLATE. THE EVENT LED TO A SIGNIFICANT DELAY OF APPROXIMATELY 25 MINUTES, AND THE FRACTURE COULD NOT BE FIXED AS REQUIRED. THERE WAS REPORTED PATIENT HARM, BUT NO ADDITIONAL MEDICAL OR SURGICAL INTERVENTION OR EXTENDED HOSPITALIZATION WAS NECESSARY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25114047 ↗
• MalfunctionMay 7, 2026Device-Device Incompatibility

  IT WAS REPORTED DURING A PPFX SURGERY THAT THE VA LOCKING PPFX GREATER TROCHANTER RING COULD NOT BE THREADED ONTO THE PROXIMAL FEMUR PLATE. ATTEMPTS TO ENGAGE A SECOND RING PLATE ALSO FAILED, RESULTING IN THE INABILITY TO IMPLANT ANY RING PLATE. THE EVENT LED TO A SIGNIFICANT DELAY OF APPROXIMATELY 25 MINUTES, AND THE FRACTURE COULD NOT BE FIXED AS REQUIRED. THERE WAS REPORTED PATIENT HARM, BUT NO ADDITIONAL MEDICAL OR SURGICAL INTERVENTION OR EXTENDED HOSPITALIZATION WAS NECESSARY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25113930 ↗
• InjuryApr 21, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE SUBJECT LIS-027 CLINICAL ADVERSE EVENTS RECEIVED FOR EXCESSIVE BLEEDING. DEVICE AND PROCEDURE(RELATEDNESS). DEVICE RELATED: RELATED TO DEVICE. PROCEDURE RELATED: RELATED TO PROCEDURE. DATE OF EVENT: JANUARY 08, 2025. DATE OF IMPLANT: (B)(6) 2025. DATE OF REVISION: NO INFORMATION PROVIDED. DEVICE LOCATION: NO INFORMATION PROVIDED. TREATMENT/IMPACT: NO INFORMATION PROVIDED. DEPUY SYNTHES PRODUCT USED: CATALOG NUMBER: 02.221.101S. LOT NUMBER: NO INFORMATION PROVIDED. COMPONENT TYPE: PLATE. DESCRIPTION: DPS - VA LOCKING PPFX GREATER TROCHANTER RING ATTACHMENT PLATE 3.5.

  Patient problems: Hemorrhage/Blood Loss/Bleeding

  MAUDE report 21874668 ↗