This page has been archived on the Web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.
JUNO DRF (2016-02-18)
- Starting date:
- February 18, 2016
- Posting date:
- March 4, 2016
- 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-57416
Affected Products
JUNO DRF
Reason
Philips has become aware that an operator got hurt while relocating a patient from Juno DRF table onto the patient's bed. Standing behind the table top between the left table top support arm and the detector holder, the operator got squeezed between the left table top support arm and the detector holder.
Affected products
JUNO DRF
Lot or serial number
ALL
Model or catalog number
9784729831
Companies
- Manufacturer
-
Villa Sistemi Medicali S.P.A.
via Delle Azalee 3
Buccinasco
20090
ITALY