CombiDiagnost R90 (2019-12-11)

Starting date:

December 11, 2019

Posting date:

January 6, 2020

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-72011

Last updated: 2020-01-07

• Reason
• Affected products

Affected Products

CombiDiagnost R90

Reason

Philips has identified through customer complaints about an error 80(limit switch hit and activated) when using the table down button to drive the table from a '+'or '-' degree tilting position back to horizontal as well as the system power distribution unit(SPDU) producing a significant amount of smoke.

Affected products