Health product recall

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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