Midmark 630-020Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841709106507), received between Jul 19, 2021 and Jul 19, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Human-Device Interface 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. How this data works · Data updated Oct 13, 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.

• InjuryJul 19, 2021Human-Device Interface Problem; Human-Device Interface Problem

  THIS REPORT SUMMARIZES AN EVENT THAT OCCURRED ON (B)(6) 2021 IN WHICH IT WAS STATED THAT A SERVICE TECHNICIAN WAS REPLACING A BASE ACTUATOR ON A PROCEDURE TABLE. WHILE SERVICING THE TABLE, THE SERVICE TECH TIPPED THE TABLE ON ITS SIDE. IN DOING SO, THE SERVICE TECHNICIAN RECEIVED A BACK INJURY. THE SERVICE TECHNICIAN IS STATED TO HAVING GONE TO PHYSICAL THERAPY FOR THE INJURY, HOWEVER, NO FURTHER INFORMATION OF THE MEDICAL ATTENTION SOUGHT IS AVAILABLE. NO FURTHER DETAILS ARE AVAILABLE AT THE TIME OF THIS REPORT.

  Patient problems: Pain

  MAUDE report 12189164 ↗