Cordis US Corp: ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 601814RMC

Hazard

There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement device is prepared.

Details from the source

Reason for recall: There is a potential for separation of the ANGIOGUARD RX / XP delivery system and capture sheath which include but are not limited to situations of an intra-procedural delay, unplanned percutaneous or surgical intervention, or stroke; while a replacement device is prepared. Distribution: Worldwide distribution. Quantity: 471 units Lot/code info: UDI/DI 20705032056745; Lot Numbers: 35263328, 35264207, 35264213, 35264216, 35265393, 35265648, 35265659

UPC codes

20705032056745

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.