Midmark 630-021Recalls & reported problems
Midmark Corporation · This procedures table is intended to be used as a chair / table to provide positioning and support of patients during general examinations and procedures conducted by qualified medical professionals in a medical office environment. · 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 00841709106514), received between Jul 8, 2025 and Jul 8, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Collapse” (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.
Reports received per month
Most reported problems
Device problems
- Collapse1
Patient problems
- Muscle/Tendon Damage1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 8, 2025Collapse; Collapse
ON JUNE 10, 2025, MIDMARK CORPORATION WAS NOTIFIED OF AN INSTANCE THAT OCCURRED ON OR AROUND (B)(6) 2023 IN WHICH A MODEL 630 PROCEDURE CHAIR FELL CAUSING THE PATIENT TO FALL TO THE GROUND. DUE TO THE DESCRIPTION OF EVENT AND DUE DILIGENCE, MIDMARK CORPORATION COMPLIED WITH FILING THIS INSTANCE.
Patient problems: Muscle/Tendon Damage
MAUDE report 22436151 ↗
Other CHAIR, SURGICAL, AC-POWERED devices
- Ritter 224-002Midmark Corporation · CHAIR, SURGICAL, AC-POWERED2 reports
- NA Shoulder ChairSteris Corporation · CHAIR, SURGICAL, AC-POWERED1 report
- Midmark 630-020Midmark 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.