• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall Fujifilm FDR Go Plus mobile Xray system

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
  Class 2 Device Recall Fujifilm FDR Go Plus mobile Xray system see related information
Date Initiated by Firm July 19, 2019
Create Date August 30, 2019
Recall Status1 Terminated 3 on August 28, 2020
Recall Number Z-2441-2019
Recall Event ID 83524
510(K)Number K080701  
Product Classification System, x-ray, mobile - Product Code IZL
Product Fujifilm FDR Go Plus mobile X-ray system
Code Information All serial numbers
Recalling Firm/
Manufacturer
Fujifilm Medical Systems U.S.A., Inc.
81 Hartwell Ave Ste 300
Lexington MA 02421-3160
For Additional Information Contact SAME
617-861-5300
Manufacturer Reason
for Recall
The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
FDA Determined
Cause 2
Software design
Action Fuji Film issued notifications via FedEx standard overnight mail on July 19, 2019 advising of the problem, health risk and action to take: During this field action, you can continue to use your current FDR Go PLUS by following these additional instructions:1. Set the monitor sleep mode to Off. Complete the Field Action Verification Form, and upon receipt FUJIFILM service personnel will contact you to schedule a visit to correct your device.FUJIFILM will correct your affected device(s) by applying a registry file to your current software version, at no cost to you.. Question contact: Field action coordinator, Jeffrey Wan, via phone at 201-675-8947 or email mailto:jeffrey.wan@fujifilm.com
Quantity in Commerce 174 units
Distribution Nationwide
Total Product Life Cycle TPLC Device Report

1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database 510(K)s with Product Code = IZL and Original Applicant = SHIMADZU CORP.
-
-