Product Wiki · Recalls · Health Canada — Medical Devices

Solero MTA System and Solero Microwave Tissue Ablation Applicator… — recall 59400

Health Canada — Medical Devices · Canada · 2019-05-10 · Type II

As described by Health Canada — Medical Devices: Solero MTA System and Solero Microwave Tissue Ablation Applicator (2019-04-16)

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
59400
Date of alert
2019-05-10
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: AngioDynamics, Inc. is conducting a field safety corrective action (FSCA), to the end user level on the Solero Microwave Tissue Ablation (MTA) system, generators and applicators. The instructions and warnings have been clarified to ensure the Solero system is functioning properly prior to starting a procedure.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/solero-mta-system-and-solero-m

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.

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