Perimeter Octopus 900 (2019-06-10)

Starting date:

June 10, 2019

Posting date:

June 21, 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-70241

Last updated: 2019-06-21

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  Reason
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  Affected products

Affected Products

Perimeter Octopus 900

Reason

When a kinetic perimetry examination is performed for both eyes, continuing the first examination will overwrite the result of the previously done second examination. An amended examination is stored for the first eye examined, with data from the first eye. The information from the second eye is lost.

Affected products