Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and manipulation prior to placement, may have loose particles within catheter lumens that may be introduced to patients, which could cause embolic event, small vessel occlusion, and subacute to chronic inflammatory response.
Reason for recall: Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and manipulation prior to placement, may have loose particles within catheter lumens that may be introduced to patients, which could cause embolic event, small vessel occlusion, and subacute to chronic inflammatory response. Distribution: US Nationwide distribution in the states of IL, AL, FL, NC, WI, GA, SC, IN, KS, CA, OH, NY, NH, CO, MA, NV, UT, TX. Quantity: 353 Lot/code info: All lots, REF/UDI-DI/Lot(Expiration): PL17-160-000/00818075010455/ 900164(8/31/2022), 900165(8/31/2022), 900172(8/31/2022), 900177(9/30/2022), 900180(9/30/2022), 900186(10/31/2022), 900187(10/31/2022), 900188(10/31/2022), 900193(10/31/2022), 900196(12/31/2022), 900199(12/31/2022), 900202(12/31/2022), 900221(2/28/2023), 900222(2/28/2023), 900225(2/28/2023), 900226(3/31/2023), 20441(11/30/2023), 20476(11/30/2023), 20650(12/31/2023); PL17-160-045/00818075010462/900167(8/31/2022), 900168(8/31/2022), 900169(8/31/2022), 900174(8/31/2022), 900175(8/31/2022), 900179(9/30/2022), 900181(9/30/2022), 900183(10/31/2022), 900185(10/31/2022), 900205(1/31/2023), 900206(1/31/2023), 900210(1/31/2023), 900211(1/31/2023), 900215(1/31/2023), 900220(1/31/2023), 900219(1/31/2023), 900217(2/28/2023), 900223(2/28/2023), 900224(2/28/2023); PL17-160-090/00818075010479/900170(8/31/2022), 900171(8/31/2022), 900178(9/30/2022), 900182(9/30/2022), 900184(10/31/2022), 900192(11/30/2022), 900195(11/30/2022), 900209(1/31/2023), 900228(3/31/2023)
00818075010455, 00818075010462, 00818075010479
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.