FDA-Device2021-09-22Class I
Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Cordis Corporation
Hazard
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.
Sold states
Worldwide distribution - US Nationwide distribution and the countries of Canada, Europe.
Affected count
45 units
Manufactured in
14201 NW 60th Ave, N/A, Miami Lakes, FL, United States
Products
Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2428-2021Don't want to check this manually?
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