Product Wiki · Recalls · Health Canada — Medical Devices

Pressure Monitoring Kit (Sterile) and Vamp Venous Arterial Blood… — recall 63016

Health Canada — Medical Devices · Canada · 2020-01-06 · Type III

As described by Health Canada — Medical Devices: Pressure Monitoring Kit (Sterile) and Vamp Venous Arterial Blood Management Protection System (2019-11-13)

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
63016
Date of alert
2020-01-06
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: This non-conformance is due to the inability to flush a disposable pressure transducer system upon the initiation of priming. If this inability to flush occurs, the clinician can obtain another transducer kit with minimal delay in set-up time. This issue occurs during setup and before use.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/pressure-monitoring-kit-steril

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.