FDA Recall Terminated

Mobile X-ray System, Model: MUX-100, MUX-100H Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannnot move and/or of outpatients in emergency

Recall: Z-1150-2014 · Initiated November 15, 2013

Recall

Recall Number
Z-1150-2014
Event Number
67353
Firm
Shimadzu Medical Systems
FEI Number
1000125362
Product Code
IZL
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
November 15, 2013
Posted
March 7, 2014
Terminated
June 25, 2015
Address
20101 S Vermont Ave, Torrance, CA, 90502-1328

Description

Mobile X-ray System, Model: MUX-100, MUX-100H Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannnot move and/or of outpatients in emergency

Reason

Shimadzu Corporation is recalling the Shimadzu Mobile X-ray Sytems (MUX-100 and MUX-100H) because the connecting metal plate which connects the main chassis and the column of MUX-100 may crack.

Action

A Field Safety Notice and an Urgent Voluntary Medical Device Recall Notice were sent to customers to inform them that SHIMADZU CORPORATION has identified a potential issue in certain manufacturing lots of the Shimadzu Mobile X-ray Systems. Customers are informed that as a result of their investigation, it has been learned that the connecting work of very few column used in specific lots for the MUX series was not done correctly, and it may cause a crack. Therefore, if the machine is continuously used in that condition, there is the possibility that the column will start to lean. The notices informs the customers of the actions to be taken. Customers are instructed to contact Shimadzu Medical Systems National Technical Support at (800) 228-1429.

Distribution

USA Nationwide Distribution

Quantity

56 units