Ritter 224-002Recalls & 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
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841709106002), received between Jul 28, 2025 and Jul 28, 2025 — classified as 2 injuries.
The most frequently reported specific device problem is “Unintended System Motion” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended System Motion2
Patient problems
- Bone Fracture(s)1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJul 28, 2025Unintended System Motion; Unintended System Motion
ON JULY 10, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND ON (B)(6) 2025, IN WHICH CLEANING PERSONNEL WERE CLEANING A MODEL 224 EXAM TABLE. WHILE CLEANING THE TABLE, THE FOOT CONTROL WAS ACTIVATED AND THE TABLE DESCENDED ONTO THEIR FOOT. MIDMARK CORPORATION HAS MADE MULTIPLE ATTEMPTS FOR FURTHER INFORMATION OF THE CURRENT STATE OF THE TABLE AND ADDITIONAL DETAILS OF THIS INSTANCE, ALTHOUGH NO FURTHER DETAILS HAVE BEEN MADE AVAILABLE.
Patient problems: Insufficient Information
MAUDE report 22639147 ↗InjuryJul 28, 2025Unintended System Motion; Unintended System Motion
ON JULY 2, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND (B)(6) 2025, IN WHICH A NURSE WAS PREPARING A PROCEDURE BED FOR A PATIENT. WHILE DOING SO, THE MODEL 224 EXAM TABLE FOOT CONTROL WAS ACTIVATED AND THE TABLE DESCENDED ONTO THE NURSE'S FOOT CAUSING AN ALLEGED BREAK TO THE RIGHT GREAT TOE. MIDMARK CORPORATION HAS MADE MULTIPLE ATTEMPTS FOR FURTHER INFORMATION OF THIS INSTANCE WITH NO FURTHER DETAILS MADE AVAILABLE.
Patient problems: Bone Fracture(s)
MAUDE report 22635093 ↗
Other CHAIR, SURGICAL, AC-POWERED devices
- NA Shoulder ChairSteris Corporation · CHAIR, SURGICAL, AC-POWERED1 report
- Midmark 630-020Midmark Corporation · CHAIR, SURGICAL, AC-POWERED1 report
- Midmark 630-021Midmark Corporation · CHAIR, SURGICAL, AC-POWERED1 report
- Ritter 225-002Midmark Corporation · CHAIR, SURGICAL, AC-POWERED1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.