Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one.
Reason for recall: Reported Outer sheath distal black tip detaching from the device can remain around the stent saddle, preventing proper expansion, resulting in prolongation of the procedure to exchange the device for a new one. Distribution: Nationwide including Puerto Rico Foreign: To be provided Quantity: 91 units (OUS) Lot/code info: GTIN: 08714729904557 Lot Numbers: 33335139, 33335340, 33336413, 33511491, 34015885, 34065661, 34068983, 34101926
08714729904557
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.