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FDA Medical Device Recalls (openFDA)

Heartware, Inc.: STERILE HVAD (HeartWare Ventricular Assist Device) PUMP (US), Model Number 1101

Recall number
Z-0476-2024
Recalling firm
Heartware, Inc.
Product
STERILE HVAD (HeartWare Ventricular Assist Device) PUMP (US), Model Number 1101
Status
Open, Classified
Initiated
2023-10-31
Posted
2023-12-02
Terminated
not on file
Reason
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
Root cause
Labeling design
Action
Heartware issued an URGENT: MEDICAL DEVICE CORRECTION notice to its consignees on 10/31/2023 via letter (UPS). The notice explained the issue and informed them of the updates to the HVAD IFU and PM (patient manual).
Quantity
380 units
Distribution
Worldwide
Lot, serial or model codes
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
510(k) numbers
not on file
PMA numbers
not on file
Product code
DSQ
Firm FEI
3007042319
Firm city
Miami Lakes
Firm state
FL
Firm country
not on file

Where this comes from

Register
FDA Medical Device Recalls (openFDA)
Publisher
U.S. Food and Drug Administration (openFDA)
File
device-recall-0001-of-0001.json.zip
sha256
b87518bfe2e8
Size
288210821 bytes
Published
2026-09-28
Read
2026-09-29T08:25:23.626Z
Source file
Source file retained · verify
Refresh due
2026-10-06

Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.

Cite as

FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28

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