Midmark 204 Manual Examination TableRecalls & reported problems
Midmark Corporation · The Midmark 204 Manual Examination Table is intended to be used as a table to provide positioning and support of patients during examination procedures conducted by qualified medical professionals in an office environment. · Class 1
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00841709106118), received between Jan 3, 2019 and Oct 15, 2020 — classified as 3 injuries.
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
- Adverse Event Without Identified Device or Use Problem3
Patient problems
- Fall3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
InjuryOct 15, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A PATIENT WAS SEATED UPRIGHT ON A RITTER 204-001 MANUAL EXAMINATION TABLE WITH THEIR BACK UNSUPPORTED AND FEET DANGLING OVER THE SIDE. AT SOME POINT DURING OR AFTER A THERAPEUTIC PHLEBOTOMY PROCEDURE, THE PATIENT INFORMED THE NURSE THAT HE WAS EXPERIENCING DIZZINESS AND WAS SWEATY. THE NURSE LEFT THE ROOM TO "GET THE PATIENT A GATORADE", AND WHILE THE NURSE WAS GONE, THE PATIENT LOST CONSCIOUSNESS AND FELL FROM THE TABLE. THE PATIENT SUSTAINED SEVERE AND SERIOUS PERSONAL INJURIES THAT REQUIRED MEDICAL AID, TREATMENT, AND ATTENTION.
Patient problems: Fall
MAUDE report 10684489 ↗InjuryMay 14, 2020Adverse Event Without Identified Device or Use Problem
AFTER A PATIENT EXAM, WHEN STEPPING DOWN FROM THE 204 EXAMINATION TABLE ONTO THE FOOTSTEP, THE PATIENT'S FOOT SLIPPED OFF THE SIDE OF THE STEP CAUSING THE PATIENT TO FALL TO THE GROUND ON THEIR SHOULDER RESULTING IN AN INJURY TO THE PATIENT'S SHOULDER AND NECK.
Patient problems: Fall
MAUDE report 10059462 ↗InjuryJan 3, 2019Adverse Event Without Identified Device or Use Problem
AFTER THE PATIENT EXAM, WHEN STEPPING DOWN FROM THE EXAM TABLE ONTO THE FOOTSTEP, THE PATIENT SLIPPED WHILE THEIR FEET WERE ON THE FOOTSTOOL AND FELL TO THE GROUND. THE PATIENT WAS TRANSPORTED TO THE EMERGENCY DEPARTMENT FOR FURTHER EVALUATION. NO FURTHER INFORMATION WAS PROVIDED REGARDING THE STATUS OF THE PATIENT.
Patient problems: Fall
MAUDE report 8214493 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.