FDA Recall Open, Classified

FDR Visionary Suite - Intended to generate digital or conventional radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts of human anatomies in all routine radiography examinations. Model/Catalog Number: 566-16130-23 566-16130-33

Recall: Z-1898-2024 · Initiated April 11, 2024

Recall

Recall Number
Z-1898-2024
Event Number
94443
Firm
FUJIFILM Healthcare Americas Corporation
FEI Number
1000513161
Product Code
KPR
Status
Open, Classified
Root Cause
Component design/selection
Initiated
April 11, 2024
Posted
May 24, 2024
Address
81 Hartwell Ave, Ste 300, Lexington, MA, 02421-3160

Description

FDR Visionary Suite - Intended to generate digital or conventional radiographic images of the skull, spinal column, chest, abdomen, extremities, and other body parts of human anatomies in all routine radiography examinations. Model/Catalog Number: 566-16130-23 566-16130-33

Reason

Bolts on the CH-200 tube may rupture due to fatigue failure, causing the tube support to fall, could result in patient injury

Action

FUJIFILM Healthcare Americas Corporation (FUJIFILM) issued Urgent -FIrst Notice letter via email on 4/11/24. Letter states reason for recall, health risk and action to take: 1)Please complete and return the form attached on page 3 of this communication. Providingthe response with the information requested is essential for ensuring appropriate action istaken 2)Please contact Customer Service at 1-888-FUJIMED (1-888-385-4633) to open a serviceticket. 3)Until your upgrade is scheduled and completed, you can continue to safely use FDRVisionary Suite, however, inspect the bolts prior to use. Please contact our field action coordinator, Chaitrali Kulkarni, via email at [email protected], if you have any further questions regarding this field action.

Distribution

US Nationwide distribution in the states of AK, CA, FL, IL, NE, NH, OH, TN, WI.

Quantity

18 units