STERILE HVAD (HeartWare Ventricular Assist Device) PUMP (US), Model Number 1101
FDA Recall #Z-0476-2024 — Class II — October 31, 2023
Product Description
STERILE HVAD (HeartWare Ventricular Assist Device) PUMP (US), Model Number 1101
Reason for Recall
Updates to the HVAD system instructions for use (IFU) and patient manual (PM) will be provided. These updates will clarify (1) the conditions under which an HVAD [Controller Fault] alarm may sound and the recommended troubleshooting actions and (2) instructions relating to the useful life of the HVAD system components
Recalling Firm
Heartware, Inc. — Miami Lakes, FL
Classification
Class II — May cause temporary or medically reversible adverse health consequences.
Product Type
Devices
Product Quantity
380 units
Distribution
Worldwide
Code Information
Serial numbers: hw1005, HW1015, HW1020, HW1021, HW1022, HW1023, HW1025, HW1028, HW1031, HW1033, HW107, HW1088, HW1089, HW1090, HW1091, HW1092, HW1138, HW1139, HW1142, HW1143, HW1144, HW1146, HW1148, HW1171, HW1183, HW1200, HW1201, HW1202, HW1203, HW1204, HW1205, HW1209, HW1211, HW1222, HW1240, HW1241, HW1242, HW1243, HW1244, HW1245, HW1246, HW1247, HW1248, HW1249, HW1250, HW1252, HW1254, HW1257, HW1258, HW1261, HW1262, HW1263, HW1264, HW1265, HW1267, hw1273, HW1276, HW1277, HW1278, HW1280, HW1283, HW1292, HW1297, HW1305, HW1306, HW1308, HW1310, HW1311, HW134, HW1397, HW1398, HW1403, HW1404, HW1415, HW1426, HW1428, HW1430, HW1434, HW1437, HW1439, HW1441, HW1452, HW1454, HW1456, HW1457, HW1461, HW1462, HW1465, HW1466, HW1488, HW1510, HW1512, HW1517, HW1524, HW1528, HW1532, HW1533, HW1534, HW1535, HW1543, HW1553, HW1555, HW1556, HW1562, HW1573, HW1574, HW1589, HW1598, HW1608, HW1612, HW1618, HW1622, HW1627, HW1629, HW1630, HW1632, HW1633, HW1634, HW1636, HW1637, HW166, HW167, HW1688, HW1689, HW1694, HW1697, HW1728, HW1729, HW1733, HW174, HW1745, HW1748, HW1750, HW1757, HW176, HW1769, HW1771, HW1772, HW1801, HW1813, HW1816, HW1817, HW1818, HW182, HW184, HW187, HW190, HW191, HW1951, HW1955, HW196, HW1963, HW198, HW199, HW200, HW201, HW202, HW204, HW207, hw209, HW210, HW211, HW212, HW213, HW214, HW216, HW217, HW220, HW221, HW224, HW226, HW227, HW229, HW230, HW233, HW236, HW239, HW240, HW247, HW249, HW250, HW251, HW253, HW254, HW255, HW256, HW257, HW258, HW260, HW261, HW262, HW263, HW277, HW278, HW279, HW281, HW282, HW284, HW286, HW290, HW292, HW296, HW297, HW298, HW299, HW303, HW304, HW305, HW310, HW313, HW314, HW317, HW319, HW321, HW323, HW324, HW328, HW330, HW335, HW336, HW337, HW338, HW339, HW344, HW346, HW347, HW348, HW363, HW378, HW379, HW380, HW381, HW382, HW383, HW384, HW405, HW406, HW415, HW425, HW430, HW431, HW433, HW440, HW441, HW442, HW444, HW446, HW447, HW454, HW456, HW466, HW467, HW468, HW469, HW474, HW475, HW479, HW481, HW482, HW484, HW486, HW488, HW490, HW492, HW494, HW497, HW498, HW500, HW505, HW506, HW525, HW526, HW527, HW528, HW529, HW530, HW531, HW534, HW535, HW536, HW555, HW556, HW557, HW560, HW561, HW562, HW563, HW564, HW567, HW568, hw575, HW577, HW578, HW581, HW583, HW584, HW585, HW590, HW591, HW600, HW602, HW603, HW608, hw609, HW610, HW622, HW623, HW626, HW628, HW633, HW635, HW636, HW640, HW643, HW644, HW645, HW646, HW650, HW658, HW659, HW660, HW661, HW678, HW691, HW692, HW693, HW694, HW739, HW741, HW748, HW749, HW764, HW768, HW770, HW785, HW795, HW796, HW798, HW801, HW815, HW816, HW817, HW819, HW820, HW821, HW822, HW823, HW824, HW825, HW826, HW827, HW857, HW858, HW861, HW863, HW865, HW867, HW877, HW885, HW886, HW887, HW888, HW889, HW891, HW901, HW917, HW919, HW920, HW921, HW922, HW923, HW928, HW932, HW933, HW936, HW943, HW947, HW978, HW979, HW980
Status
Ongoing
Voluntary / Mandated
Voluntary: Firm initiated
What Should You Do?
Stop using this medical device immediately and consult your healthcare provider. Contact the recalling firm for instructions on return or replacement. If you experienced an adverse event, inform your doctor.