Health product recall

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

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

Perimeter Octopus 900

Lot or serial number

1301
1303
4816

Model or catalog number

1803000

Companies
Manufacturer
Haag-Streit, AG
Gartenstradtstrasse, 10
Koniz
3098
SWITZERLAND