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
FDA Recall Z-1898-2024 · Posted 2024-05-24
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Recalling FirmFUJIFILM Healthcare Americas Corporation
Recall StatusOpen, Classified
Product CodeKPR
Date Initiated2024-04-11
Product Quantity18 units
Reason for Recall
Bolts on the CH-200 tube may rupture due to fatigue failure, causing the tube support to fall, could result in patient injury
Firm 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.
Root Cause
Component design/selection
Distribution Pattern
US Nationwide distribution in the states of AK, CA, FL, IL, NE, NH, OH, TN, WI.
Related FDA 510(k) Records
Devices referenced by this recall via K-numbers.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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