Product Wiki · Recalls · Health Canada — Medical Devices

Vivid™ Ultrasound Systems — recall 73871

Health Canada — Medical Devices · Canada · 2023-06-23 · 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
73871
Date of alert
2023-06-23
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: GE Healthcare has become aware that certain Vivid™ Ultrasound Systems may not boot up in a timely fashion. If this occurs, it can delay availability of the device in timecritical emergency situations. Recall start date : June 12, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/vividtm-ultrasound-systems

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.