Other Medical Devices

As the temperature and time out of range was exceeded, product performances cannot be guaranteed

Specific lots have not been irradiated to eliminate pyronema and therefore the sterility of the affected products may be compromised.

Distribution without Pre-Market Clearance

Distribution without Pre-Market Clearance

Distribution without Pre-Market Clearance

Distribution without Pre-Market Clearance

mislabeled product

Reports of Polyurethane Displacement in the dialyzer, and might be identified as a blood leak

During internal testing (at manufacturer site) of two torque wrench devices, it was detected that the torque limiting function was out of specification. The specified torque limiting value is 12 Nm. The measuring results for both instruments were 4 Nm.

Reports of Polyurethane Displacement in the dialyzer, and might be identified as a blood leak

Over time, the driveline cover may become hardened, creating difficulty or an inability to slide the cover back to access the driveline to controller connector. Access to the driveline connector may be delayed, which may result in patient harm from a prolonged pump stop, if an urgent driveline connection or controller issue needs to be addressed. In the event a hardened driveline cover is observed, contact your Medtronic field representative for further assessment and/or servicing.

The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.

Over time, the driveline cover may become hardened, creating difficulty or an inability to slide the cover back to access the driveline to controller connector. Access to the driveline connector may be delayed, which may result in patient harm from a prolonged pump stop, if an urgent driveline connection or controller issue needs to be addressed. In the event a hardened driveline cover is observed, contact your Medtronic field representative for further assessment and/or servicing.

The firm has received complaints of the device becoming hot. The firm has updated the user manual to include warnings that applied parts in contact with the patient may in some situations exceed 41 degrees Celsius (105.8 degrees Fahrenheit), clarification on expected service life, and the need for maintenance to certain components.

Affected lots of the product are being recalled due to potential microbial growth in the fluid inside the device. if a compromised product is used by a child with a weakened immune system, an infection or other illness could occur.

The BIOLOX Delta Ceramic Head size 36XL is labelled as the size 32XL and vice-versa.

(1)Software version 2.74 upgrade and (2)hardware related cause that affects only CDX Machines, has been identified as the UI-MICs Board is sensitive to Electromagnetic Interference (EMI) which will cause the false alarm "Remove USB 2 Device".

Reports of an increase in reactive negative controls and false positive results with certain lots of Alinity M Resp-4-Plex AMP kits.

Reports of an increase in reactive negative controls and false positive results with certain lots of Alinity M Resp-4-Plex AMP kits.

Potential for Internal Blood Leaks due to a twisted gasket in the dialyzer