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: 118 units (OUS) Lot/code info: GTIN: 08714729976684 Lot Numbers: 32878539, 33336847, 33338446, 33775901, 33795273, 33900261, 33900262, 34076575, 34083270, 34172108, 34172109
08714729976684
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.