Ventana HE 600 System (2019-10-30)

Starting date:

October 30, 2019

Posting date:

November 15, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type II

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-71617

Last updated: 2019-11-15

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  Reason
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  Affected products

Affected Products

Ventana HE 600 System

Reason

Situation related to potential burnt coverslip module on the Ventana HE600 system (Cat # 06917259001). A leak in the staining module caused an electrical short and damage to the electrical component.

Affected products