πŸ”¬

Diagnostic Equipment

πŸ₯ Medical Devices β€’ 6,627 recalls

A shipment to Guadeloupe suffered a temperature excursions up to 47.8ΒΏC, exceeding the acceptable limits. After detection of the issue, Global Supply Chain QA asked the bioMΒΏrieux distributor in Guadeloupe to put products in quarantine in July 2017; After several reminders, the distributor informed in November 2017 that products were delivered to customers.

Mar 23, 2018 Diagnostic Equipment View Details β†’

The firm will be updating the Instructions for Use for the product. Current IFUs instruct users to lower the primary bag 20 inches below the secondary bag using a hanger when performing a secondary infusion. However, the firm supplies 12.5-inch hangers with the Baxter disposable secondary sets.

May 8, 2018 Diagnostic Equipment Nationwide View Details β†’

Users have misinterpreted the display for out of range measurement indicated by the blinking" ---" to mean a zero measurement.

May 15, 2018 Diagnostic Equipment Nationwide View Details β†’

Potential that one or more image series may be missing from an exam without a user warning displayed in the Viewer.

Jan 25, 2018 Diagnostic Equipment Nationwide View Details β†’

The firm will be updating the Instructions for Use for the product. Current IFUs instruct users to lower the primary bag 20 inches below the secondary bag using a hanger when performing a secondary infusion. However, the firm supplies 12.5-inch hangers with the Baxter disposable secondary sets.

May 8, 2018 Diagnostic Equipment Nationwide View Details β†’

Users have misinterpreted the display for out of range measurement indicated by the blinking "-0-" to mean a zero measurement

May 15, 2018 Diagnostic Equipment Nationwide View Details β†’

While in Full Disclosure playback, a user may inadvertently close the Full Disclosure Control Window using the ESC key function, instead of pressing the X icon in the upper right corner of this window.

Nov 20, 2017 Diagnostic Equipment Nationwide View Details β†’

Report was of an interrupted MR scan after patient complained about acoustic distortion, and heat felt form the headphones.

Oct 28, 2017 Diagnostic Equipment Nationwide View Details β†’

Replacement of units lacking an updated device approval.

May 8, 2018 Diagnostic Equipment View Details β†’

The bug causes BOLD activation maps to be visualized as overlays without taking the coregistration into account. Any output created from these activation maps as overlays will not be adjusted according to the coregistration.

Jul 3, 2015 Diagnostic Equipment Nationwide View Details β†’

Potential that one or more image series may be missing from an exam without a user warning displayed in the Viewer.

Jan 25, 2018 Diagnostic Equipment Nationwide View Details β†’

There is an error related to the relative geometry between fiber tracts in a fiber group and images. The error occurs in the following situations: A group of fibers has been selected using the VOI functionality and put into a fiber group. This is done with images series A visualized in the 3D viewer. Then a new images series B is visualized in the 3D viewer. If image series A and B have the same geometrical resolution (pixel sizes and slice distances), the coregistration matrix taking A to B will not be applied to the fiber group, and therefore the fiber group will in general not be positioned correctly on B in the 3D viewer. Furthermore, if the fiber group is exported as a new image series the fibers could be misplaced, and similarly if the fibers are visualized in the MPR on B, the positioning will not be correct. The misalignment will be equal to the rotations/translations necessary to align A with B.

Dec 21, 2012 Diagnostic Equipment Nationwide View Details β†’

An error was discovered in the interpretation of certain DICOM header tags that may lead to incorrect orientation labeling, and thus and indirect left-right, up-down or anterior-posterior flipping of images.

Dec 15, 2014 Diagnostic Equipment Nationwide View Details β†’