Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
Reported: September 22, 2021 Initiated: July 21, 2021 #Z-2429-2021
Product Description
Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
Reason for Recall
Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.
Details
- Recalling Firm
- Cordis Corporation
- Units Affected
- 1610 units
- Distribution
- Worldwide distribution - US Nationwide distribution and the countries of Canada, Europe.
- Location
- Miami Lakes, FL
Frequently Asked Questions
What product was recalled? ▼
Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB. Recalled by Cordis Corporation. Units affected: 1610 units.
Why was this product recalled? ▼
Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on September 22, 2021. Severity: Critical. Recall number: Z-2429-2021.
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