Product Wiki · Recalls · Health Canada — Medical Devices

Zenith Slide W-I-D-E Long Term Care Bed (Models 9000 and 7000)… — recall 52476

Health Canada — Medical Devices · Canada · 2014-10-01 · Type III

As described by Health Canada — Medical Devices: Zenith Slide W-I-D-E Long Term Care Bed (Models 9000 and 7000) (2014-07-28)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
52476
Date of alert
2014-10-01
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: 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.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/zenith-slide-w-e-long-term-car

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