T7 Zipper Toga recall in Canada: Sterility issues
In plain language
This recall involves T7 Zipper Toga surgical devices sold in Canada. They are being recalled because some shipments were expired, which could compromise their sterility. Healthcare professionals should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
- Check the lot and model numbers of your T7 Zipper Toga devices.
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Affected products
T7 Zipper Toga
Model: 0416830100, 0416840100
Lot: 21137372, 21137492, 21152132, 21277472
Why this matters
Sterility issues
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: 21137372, 21137492, 21152132, 21277472
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 0416830100, 0416840100
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 issues
What should consumers do?
Contact the manufacturer if you require additional information. Check the lot and model numbers of your T7 Zipper Toga devices.
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 issues
When was this product recalled?
This product was recalled on November 20, 2025.
Is the GE Healthcare GmbH brand affected by this recall?
Yes, GE Healthcare GmbH products are affected by this recall. This recall involves T7 Zipper Toga surgical devices sold in Canada. They are being recalled because some shipments were expired, which could compromise their sterility. Healthcare professionals should contact the manufacturer for more information.