This page has been archived on the Web
Information identified as archived is provided for reference, research or recordkeeping purposes. It is not subject to the Government of Canada Web Standards and has not been altered or updated since it was archived. Please contact us to request a format other than those available.
ALLURA XPER FD20/20 (2015-10-02)
- Starting date:
- October 2, 2015
- Posting date:
- October 22, 2015
- 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-55518
Affected Products
ALLURA XPER FD20/20
Reason
Philips Healthcare a découvert, grâce aux commentaires de ses clients et à des contrôles internes, une défaillance logicielle pouvant mener à une interruption intermittente et à court terme de la fonction de radioscopie.
Affected products
ALLURA XPER FD20/20
Lot or serial number
All lots.
Model or catalog number
ALLURA XPER FD20/20
Companies
- Manufacturer
-
Philips Medical Systems Nederland B.V.
Veenpluis 4-6
Best
5684
NETHERLANDS