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Health product recall

Platinum (DRF) - Foot Rest(2013-07-01)

Starting date:
July 1, 2013
Posting date:
September 19, 2013
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-35741

Recalled Products

Platinum (DRF) - Foot Rest

Reason

A user error while setting up the foot rest has been observed that may result in patient injury.

Affected products

Platinum (DRF) - Foot Rest

Lot or serial number

Not applicable

Model or catalog number
  • 6F
Companies
Manufacturer
Apelem Sa
Rue Georges Besse
Allee Von Neumann, Nimes
30900
FRANCE