Class II
Medical Device Recall: Shimadzu, Trinias, Digital Angiography System
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION · January 29, 2024
Reason for Recall
Due to capacitor manufacturing issue, their is a potential that Flat Panel Device may have abnormal display or no function.
Distribution
US Nationwide distribution in the states of OH.
States Affected
NATIONWIDE
Quantity Affected
1
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1292-2024
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.