Product Wiki · Recalls · Health Canada — Medical Devices

Intellispace Portals - DX and HX (2014-03-11) — recall 51520

Health Canada — Medical Devices · Canada · 2014-04-04 · Type II

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
51520
Date of alert
2014-04-04
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: During Spect reconstructions using attenuation correction and scatter correction, no scatter correction is being applied in the Autospect Pro application on Intellispace portal with software version 5 and 6. Resolution recovery is not applied correctly in Spect reconstructions using Astonish in Autospect Pro on Intellispace portal unless the data is acquired with VXGP collimators.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/intellispace-portals-dx-and-hx

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

Related

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.