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
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
CombiDiagnost R90
Lot or serial number
Not applicable.
Model or catalog number
709030
Companies
- Manufacturer
-
Philips Medical Systems DMC GmbH
Rontgenstrabe 24
Hamburg
22335
GERMANY