Skip to content

Ritter 225-002Recalls & reported problems

Midmark Corporation · The examination table is intended to be used as a chair / table to provide positioning and support of patients during general examination procedures conducted by medical professionals. · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841709105975), received between Sep 16, 2022 and Sep 16, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Improper or Incorrect Procedure or Method” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Improper or Incorrect Procedure or Method1

Patient problems

  • Bone Fracture(s)1

Recent adverse event reports

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

  • InjurySep 16, 2022Improper or Incorrect Procedure or Method; Improper or Incorrect Procedure or Method

    THIS REPORT SUMMARIZES AN EVENT THAT OCCURRED ON OR AROUND (B)(6) 2022, IN WHICH IT WAS STATED THAT A NURSE HAD THE FOOT CONTROL RIGHT IN FRONT OF THE CHAIR BASE WHILE LOWERING THE BASE AND DID NOT REMOVE HER FOOT FROM THE CONTROL WHEN LOWERING THE CHAIR. THE SHROUDS LOWERED ONTO HER TOE AND FRACTURED HER TOE.

    Patient problems: Bone Fracture(s)

    MAUDE report 15438015 ↗

Other CHAIR, SURGICAL, AC-POWERED devices

All CHAIR, SURGICAL, AC-POWERED devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.