Perimeter Octopus 900 recall in Canada: Medical device data error
In plain language
This recall involves the Perimeter Octopus 900 medical device sold in Canada. It's being recalled because it may lose data from eye examinations. Healthcare professionals should stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Check model and serial numbers.
- Follow instructions from Health Canada for return or repair.
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Affected products
Perimeter Octopus 900
Model: 1803000
Lot: 1301, 1303, 4816
Why this matters
Medical device data error
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 1301, 1303, 4816
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 1803000
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Medical device data error
What should consumers do?
Stop using the product immediately. Check model and serial numbers. Follow instructions from Health Canada for return or repair.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Medical device data error
When was this product recalled?
This product was recalled on June 21, 2019.
Is the Perimeter brand affected by this recall?
Yes, Perimeter products are affected by this recall. This recall involves the Perimeter Octopus 900 medical device sold in Canada. It's being recalled because it may lose data from eye examinations. Healthcare professionals should stop using the product and follow the return/repair steps in the official notice.