This page has been archived on the Web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.

Archived

This page has been archived on the Web.

Health product recall

APOLLO AND JUNO DRF (2016-02-17)

Starting date:
February 17, 2016
Posting date:
April 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-57736

Affected products

  1. APOLLO-MAIN UNIT
  2. JUNO DRF

Reason

An operator got hurt while relocating a patient from table onto the patient's bed. Standing behind the table top between the left table top support arm and the detector holder, he got squeezed between the left table top support arm and the detector holder.

Affected products

  1. APOLLO-MAIN UNIT

Lot or serial number
  • S/N 08060167
  • S/N 08070501
Model or catalog number
  • 9784AXBYVT
Companies
Manufacturer
Villa Sistemi Medicali S.P.A.
via Delle Azalee 3
Buccinasco
20090
ITALY

B. 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

Date modified: