Integre Pro recall in Canada: Medical device performance issue
In plain language
This recall involves the Integre Pro medical device sold in Canada. It's being recalled because of a potential performance issue where a scattered laser beam may exit incorrectly. Healthcare professionals should stop using the product and follow the return steps in the official notice.
What to do
- Stop using the product immediately.
- Contact CLARION MEDICAL TECHNOLOGIES INC.
- Check for model number LP5532 and serial number IPG0542.
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Affected products
Integre Pro
Model: LP5532
Lot: IPG0542
Why this matters
Medical device performance issue
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: IPG0542
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: LP5532
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 performance issue
What should consumers do?
Stop using the product immediately. Contact CLARION MEDICAL TECHNOLOGIES INC. Check for model number LP5532 and serial number IPG0542.
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 performance issue
When was this product recalled?
This product was recalled on April 5, 2023.
Is the Ellex Medical Pty Ltd brand affected by this recall?
Yes, Ellex Medical Pty Ltd products are affected by this recall. This recall involves the Integre Pro medical device sold in Canada. It's being recalled because of a potential performance issue where a scattered laser beam may exit incorrectly. Healthcare professionals should stop using the product and follow the return steps in the official notice.