Cordis US Corp: ANGIOGUARD RX / XP Emboli Capture Guidewire System, REF 401814RMC

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: 283 units Lot/code info: UDI/DI 20705032053508; Lot Numbers: 35262517, 35263334, 35264204, 35264222, 35265345.

UPC codes

20705032053508

Source

Official record: FDA (Device enforcement) ↗

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