Orthopedic Extension 1850992Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887761972209), received between Dec 13, 2024 and Dec 13, 2024 — classified as 1 injury.

The most frequently reported specific device problem is “Use of Device Problem” (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 16, 2026.

Most reported problems

Recent adverse event reports

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

• InjuryDec 13, 2024Use of Device Problem; Use of Device Problem

  IT WAS REPORTED THAT WHILE A STAFF MEMBER WAS ATTEMPTING TO REMOVE THE EXTENSION ADAPTER ACCESSORY DEVICE FROM THE PST 500 SURGICAL TABLE, THE STAFF MEMBER SUSTAINED A FRACTURED PINKY FINGER. THE CUSTOMER REPORTED THAT THE LEVER (CONTROL HANDLE) OF THE ADAPTER WAS SO TIGHT THAT WHEN THE STAFF MEMBER ATTEMPTED TO REMOVE THE ADAPTER DEVICE WITH FORCE, THE STAFF MEMBER¿S HAND HIT ANOTHER PART WITH EXCESSIVE FORCE AND BROKE A BONE (PINKY FINGER). THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT #(B)(4).

  Patient problems: Bone Fracture(s)

  MAUDE report 20923359 ↗