Ventana HE 600 Wash (2019-10-29)

Starting date:

October 29, 2019

Posting date:

November 15, 2019

Type of communication:

Medical Device Recall

Subcategory:

Medical Device

Hazard classification:

Type III

Source of recall:

Health Canada

Issue:

Medical Devices

Audience:

General Public, Healthcare Professionals, Hospitals

Identification number:

RA-71619

Last updated: 2019-11-15

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  Reason
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  Affected products

Affected Products

Ventana HE 600 Wash

Reason

Following few customer complaints that reported loss of eosin stain while using the Ventana HE 600 wash of lot number F11147, the manufacturer requested that customers discontinue the use of this affected lot. This lot was imported in Canada, but was never distributed to any customers. The manufacturer advised us of this on 22 Oct 2019.

Affected products