Product Wiki · Recalls · Health Canada — Medical Devices

Esaote PA230E Transducer used with Esaote MyLab Systems — recall 52347

Health Canada — Medical Devices · Canada · 2014-09-25 · Type II

As described by Health Canada — Medical Devices: Esaote PA230E Transducer used with Esaote MyLab Systems - MyLab 30CV Ultrasound, MyLab 50X Vision, MyLab 25 Ultrasound, MyLab 50CV Ultrasound, MyLab 30 Gold and Phased Array Probes (2014-08-25)

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
52347
Date of alert
2014-09-25
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: Using the PA230E transducer with a user-defined setting with the output power to 100% (max) in 2D-TEI mode focusing at maximum depth, could cause the transducer surface temperature to exceed the maximum allowable limit.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/esaote-pa230e-transducer-used-

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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