Pentacam® AXL Wave and Myopia Master®
Brand(s)
Last updated
Summary
Product
Pentacam® AXL Wave and Myopia Master®
Issue
Medical devices - Performance
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
Affected products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Pentacam® AXL Wave |
Serial Number 70020 4041 2221 |
70020 |
Myopia Master® |
Serial Number 68120 8411 0221 |
68120 |
Issue
We have found an insufficient anti-reflective coating on an optical component, which can under certain circumstances lead to an additional axis length signal. If the correct axis length signal is weaker, an incorrect axis length value can be displayed.
Recall start date: August 11, 2023
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Ophthalmology
Companies
Oculus Optikgeraete GmbH
Muenchholzhaeuser Strasse 29, Wetzlar, Germany, 35582
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-74195
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