Product Wiki · Recalls · U.S. FDA — Device Enforcement

Captus 4000e Thyroid Uptake System, Model Numbers 5430-30151 and 5430-30152 - Product Usage: is intended to be used by trained nuclear Medicine Technologists or Nuclear Medicine Physicians to perform Thyroid Uptake Procedures. — recall Z-1564-2020

U.S. FDA — Device Enforcement · United States · 2020-03-03 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1564-2020
Date of alert
2020-03-03
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Capintec Inc
Product category
device
Product type
Devices
Reported risk: It is possible that the collimators have screw hole locations that were insufficiently tapped. There is a potential for the collimator assembly to fall and come into contact with a patient or operator.
Primary source: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?start_search=1&

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