EasyFuseRecalls & reported problems across all models

We found 2 models of EasyFuse by Wright Medical Technology, Inc. in the FDA's device registry (GUDID). Together they are named in 1 adverse event report in the FDA's MAUDE database, received between Apr 24, 2023 and Apr 24, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (1 report).

1 FDA recall record name at least one of these models by its device identifier.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

EasyFuse recalls

FDA recall records that name at least one of these models by its device identifier, newest first. Each recall usually covers specific models or lots, so check the details.

1. Mar 10, 2022Terminated

   The drill and adjustable drill guide can jam/bind intraoperatively resulting in the drill guide breaking.

   Z-0853-2022 · Root cause: Device Design · Recall details · FDA record ↗

Most reported EasyFuse problems

EasyFuse models

2 models, most reported first. Each model has its own page with its reports, recalls and device details.

• EasyFuse FFSP1530

  Orthopedic manual surgical instrument
  1 recall0 reports
• EasyFuse™ FFS4MTPS

  Staple, fixation, bone
  1 report

Recent EasyFuse adverse event reports

The 1 most recent reports across all models, in the reporter's own words as published by the FDA.

• MalfunctionApr 24, 2023Break; Fracture; Break; Fracture

  IT WAS REPORTED THAT THERE WAS A REVISION SURGERY. THE MTP STAPLE WAS IMPLANTED BUT NEEDED TO BE REPOSITIONED. WHEN TAKEN OUT AND RELOADED ON TO IMPLANT CARTRIDGE, THE CARTRIDGE SNAPPED AND BECAME UNABLE TO USE.

  Patient problems: Insufficient Information

  MAUDE report 16800826 ↗

Other Wright Medical Technology, Inc. products

• INFINITY51 models · 733 reports · 3 recalls
• INBONE56 models · 365 reports · 4 recalls
• INFINITY ADAPTIS8 models · 219 reports
• ORTHOLOC 3Di23 models · 28 reports · 2 recalls
• INFINITY BIOFOAM 3D5 models · 118 reports
• INFINITY EVERLAST20 models · 111 reports
• EVOLVE14 models · 28 reports · 1 recall
• SWANSON12 models · 17 reports · 1 recall