MULTIX Impact C 11020896Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04056869262147), received between May 18, 2022 and Mar 18, 2026 — classified as 1 injury, 2 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMar 18, 2026Key or Button Unresponsive/not Working

  SIEMENS HEALTHINEERS WAS NOTIFIED OF A PROBLEM INVOLVING THE MULTIX IMPACT C SYSTEM. DURING THE PRE-USE PREPARATION, THE USER FOUND THE E-STOP AT TABLETOP WAS BROKEN AND LOST ITS FUNCTION. THERE WAS NO INJURY REPORTED. ALTHOUGH THERE ARE OTHER EMERGENCY STOPS THAT CAN BE USED IF NEEDED, IN A WORST-CASE SCENARIO, CRITICAL INJURY COULD OCCUR DUE TO COLLISION IF THE USER IS UNABLE TO STOP THE TABLE USING THE OTHER EMERGENCY STOPS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24629187 ↗
• MalfunctionOct 31, 2022Installation-Related Problem; Installation-Related Problem

  SIEMENS BECAME AWARE ON AN INCIDENT WITH THE MULTIX IMPACT C UNIT. THE USER'S FINGER WAS CUT BY A SHARP EDGE OR CORNER WHEN PULLING OUT THE TRAY OF THE BUCKY WALL STAND (BWS). NO MEDICAL INTERVENTION WAS REQUIRED.

  Patient problems: Unspecified Tissue Injury

  MAUDE report 15698338 ↗
• InjuryMay 18, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

  SIEMENS BECAME AWARE OF AN INCIDENT THAT OCCURRED ON THE MULTIX IMPACT C DEVICE. WHEN THE X-RAY TECHNICIAN WAS PREPARING FOR A SCOLI SERIES EXAMINATION AT THE WALL STAND, HE NEITHER REMOVED THE STRETCH GRIP NOR CHECKED WHETHER THE OVERHEAD HAND GRIP WAS FIRMLY ATTACHED TO THE WALL STAND. AS THE EXAMINATION BEGAN, THE STRETCH GRIP CAUGHT THE TOP OF THE MULTI PURPOSE ORTHO STAND CAUSING THE HANDLE TO BECOME LOOSE AND FALL FORWARD. THE PART FELL BUT MISSED THE PATIENT. THERE ARE NO INJURIES ATTRIBUTED TO THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 14427378 ↗