This page has been archived on the Web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.

Health product recall

Zenith Slide W-I-D-E Long Term Care Bed (Models 9000 and 7000) (2014-07-28)

Starting date:
July 28, 2014
Posting date:
October 1, 2014
Type of communication:
Medical Device Recall
Subcategory:
Medical Device
Hazard classification:
Type III
Source of recall:
Health Canada
Issue:
Medical Devices
Audience:
General Public, Healthcare Professionals, Hospitals
Identification number:
RA-41591

Recalled Products

Zenith Slide W-I-D-E Long Term Care Bed (Models 9000 and 7000) 

Reason

GF Health Products, Inc / Basic American Medical Products has identified a potential issue associated with the head deck of the slide W-I-D-E beds built in November 21, 2012 and June 6th, 2014. The affected beds have the potential to experience a tubular component yielding over time creating a non-functioning head section.

Affected products

Zenith Slide W-I-D-E Long Term Care Bed (Models 9000 and 7000) 

Lot or serial number

1169000826

262678671430710

Model or catalog number

APS98674

ZZ78674

Companies
Manufacturer

GF Health Products, Inc.

2935 Northeast Parkway, Suite C,

Atlanta

30360

Georgia

UNITED STATES