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Cordis Corporation Recall 88372

Description: Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB

Cordis Corporation Recall 88372 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberZ-2428-2021
Event ID88372
Event DescriptionCordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Product TypeDevices
DistributionWorldwide distribution - US Nationwide distribution and the countries of Canada, Europe.
Quantity45 units
Recall ReasonCordis 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.
Device Classification20210922
Device Code InfoAll codes
Center Classification Date20210915
Recall Initiation Date20210721
Recalling FirmCordis Corporation
Initial Notification Letter
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