Trevo Microcatheters and Synchro Devices recall in Canada: Sterility issue
In plain language
This recall involves Trevo Microcatheters and Synchro Devices sold in Canada. They are being recalled because they may not meet sterility standards. Contact the manufacturer for more information.
What to do
- Contact the manufacturer, Stryker Neurovascular, for additional information.
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Affected products
Trevo Trak 21 Microcatheter
Lot: 136915, 140598, 136914, 119461, 140512, 136913, 90338
Trevo Pro 14 Microcatheter
Lot: 130285, 129882, 90231
Synchro Neuro Guidewire
Model: M00313010, M00316310
Lot: 123364, 123851
Why this matters
Sterility 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: 123364, 123851, 130285, 129882, 90231, 136915, 140598, 136914, 119461, 140512, 136913, 90338
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: M00313010, M00316310
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?
Sterility issue
What should consumers do?
Contact the manufacturer, Stryker Neurovascular, for 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?
Yes, there may be a health risk. Sterility issue
When was this product recalled?
This product was recalled on August 14, 2024.
Is the Stryker Neurovascular brand affected by this recall?
Yes, Stryker Neurovascular products are affected by this recall. This recall involves Trevo Microcatheters and Synchro Devices sold in Canada. They are being recalled because they may not meet sterility standards. Contact the manufacturer for more information.