Baxter Flo-Thru, Flo-Rester and Vascular Probe
Last updated
Summary
Product
Baxter Flo-Thru, Flo-Rester and Vascular Probe
Issue
Medical devices - Labelling and packaging
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number | ||
|---|---|---|---|---|
| Flo-Thru Intraluminal Shunt | All lots. | FT-12100 FT-12125 FT-12200 FT-12150 FT-12175 | ||
| Flo-Rester Disposable Internal Vessel Occluder | All lots. | 50200 50100 50125 50175 50150 | ||
| Vascular Probe Intravascular Probe | All lots. | 7152025ES 7151015ES | ||
| Vascular Probe Intravascular Probe | All lots. | 7081520 7081015 7451015 |
Issue
Baxter is issuing an important product information letter to communicate that the surgical tools education deck (ref ca-as20-220001) that may have been presented for the products listed, contains inaccurate content that does not align with the products' instructions for use (IFU).
Recall start date: February 26, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
| Synovis Life Technologies, Inc. A Subsidiary Of Baxter International Inc |
| 2575 University Avenue. W., St-Paul, Minnesota, United States, 55114-1024 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75204
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