Eclipse™ Pro and Eclipse™ Mini recall in Canada: labelling and packaging issue
In plain language
This recall involves Eclipse™ Pro and Eclipse™ Mini medical devices sold in Canada. They are being recalled because of mismatched serial numbers between the label and what is programmed in the devices. Contact the manufacturer for more information.
What to do
- Contact Spacelabs Healthcare Inc. if you require additional information.
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Affected products
Eclipse™ Mini Diagnostic Patch Recorder
Model: 98900
Lot: More than 10 numbers, contact manufacturer.
Eclipse™ Pro Ambulatory ECG And Patch Recorder
Model: 98700
Lot: More than 10 numbers, contact manufacturer.
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: 98700, 98900
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?
This recall involves Eclipse™ Pro and Eclipse™ Mini medical devices sold in Canada. They are being recalled because of mismatched serial numbers between the label and what is programmed in the devices. Contact the manufacturer for more information.
What should consumers do?
Contact Spacelabs Healthcare Inc. if you require additional information.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on January 8, 2025.
Is the Spacelabs Healthcare Inc. brand affected by this recall?
Yes, Spacelabs Healthcare Inc. products are affected by this recall. This recall involves Eclipse™ Pro and Eclipse™ Mini medical devices sold in Canada. They are being recalled because of mismatched serial numbers between the label and what is programmed in the devices. Contact the manufacturer for more information.