Stryker Bipolar Forceps and Generator recall in Canada: labelling error
In plain language
This recall involves Stryker Bipolar Forceps and Generator products sold in Canada. They are being recalled because of an error on the product label's expiration date. Healthcare professionals should contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer if you require additional information.
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Affected products
Specific affected products are listed in the official notice.
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
This recall involves Stryker Bipolar Forceps and Generator products sold in Canada. They are being recalled because of an error on the product label's expiration date. Healthcare professionals should contact the manufacturer for more information.
What should consumers do?
Stop using the product immediately. Contact the manufacturer 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 September 11, 2023.
Is the Stryker Instruments brand affected by this recall?
Yes, Stryker Instruments products are affected by this recall. This recall involves Stryker Bipolar Forceps and Generator products sold in Canada. They are being recalled because of an error on the product label's expiration date. Healthcare professionals should contact the manufacturer for more information.