Baxter Flo-Thru, Flo-Rester and Vascular Probe recall in Canada: labelling issue
In plain language
This recall involves Baxter Flo-Thru, Flo-Rester, and Vascular Probe medical devices sold in Canada. They are being recalled because the educational materials contain inaccurate content that does not align with the products' instructions for use. Healthcare professionals should contact the manufacturer for additional information.
What to do
- Contact the manufacturer if you require additional information.
Get alerts for recalls like this
Get email alerts when new recalls affect products in this category.
Affected products
Flo-Thru Intraluminal Shunt
Model: FT-12100, FT-12125, FT-12150, FT-12175, FT-12200
Lot: All lots
Flo-Rester Disposable Internal Vessel Occluder
Model: 50100, 50125, 50150, 50175, 50200
Lot: All lots
Vascular Probe Intravascular Probe
Model: 7081015, 7081520, 7151015ES, 7152025ES, 7451015
Lot: All lots
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 50100, 50125, 50150, 50175, 50200, 7081015, 7081520, 7151015ES, 7152025ES, 7451015, FT-12100, FT-12125, FT-12150, FT-12175, FT-12200
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 Baxter Flo-Thru, Flo-Rester, and Vascular Probe medical devices sold in Canada. They are being recalled because the educational materials contain inaccurate content that does not align with the products' instructions for use. Healthcare professionals should contact the manufacturer for additional information.
What should consumers do?
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 March 8, 2024.
Is the Synovis Life Technologies, Inc. A Subsidiary Of Baxter International Inc brand affected by this recall?
Yes, Synovis Life Technologies, Inc. A Subsidiary Of Baxter International Inc products are affected by this recall. This recall involves Baxter Flo-Thru, Flo-Rester, and Vascular Probe medical devices sold in Canada. They are being recalled because the educational materials contain inaccurate content that does not align with the products' instructions for use. Healthcare professionals should contact the manufacturer for additional information.