MERGE EYE STATION recall in Canada: electrical shock risk
In plain language
This recall involves the MERGE EYE STATION medical device sold in Canada. It's being recalled because certain parts may have electrical output that exceeds safety limits, posing an electrical shock risk. Stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact Merge Healthcare Incorporated for instructions.
- Return the product as instructed.
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Affected products
MERGE EYE STATION
Model: MERGE EYE STATION
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Electrical shock risk
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: More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: MERGE EYE STATION
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?
Electrical shock risk
What should consumers do?
Stop using the product immediately. Contact Merge Healthcare Incorporated for instructions. Return the product as instructed.
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. Electrical shock risk
When was this product recalled?
This product was recalled on August 9, 2019.
Is the MERGE EYE STATION brand affected by this recall?
Yes, MERGE EYE STATION products are affected by this recall. This recall involves the MERGE EYE STATION medical device sold in Canada. It's being recalled because certain parts may have electrical output that exceeds safety limits, posing an electrical shock risk. Stop using the product and follow the return steps in the official notice.