FDA Device recall Z-1142-2025

Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026

FDA Device
Class I
ongoing
Published 2025-02-26

On 2025-02-26 the FDA classified a Class I recall of Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026 by Philips Medical Systems Nederland B V, citing possibility of the patient falling from the table related to the mattress used on the patient table.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1142-2025
Classification	Class I
Status	ongoing
Initiated	2025-01-13
Published	2025-02-26
Last updated	2026-09-13 11:57 UTC
Company	Philips Medical Systems Nederland B V
Distribution	US

Product

Allura Xper FD10 - Catalog numbers: (1) 722003, (2) 722010, (3) 722026,

Reason

Possibility of the patient falling from the table related to the mattress used on the patient table.

Identifiers

code_info	Catalog numbers: (1) 722003, (2) 722010, (3) 722026; UDI-DI: (1) No UDI, (2) 00884838059030, (3) 00884838054189; Serial… Catalog numbers: (1) 722003, (2) 722010, (3) 722026; UDI-DI: (1) No UDI, (2) 00884838059030, (3) 00884838054189; Serial Numbers: (1) 285, 1634, 1349, 1153, 1154, 1472, 803, 1694, 1599, 1460, 1138, 1532, 940, 1214, 1627, 1728, 1189, 1311, 1700, 1187, 1222, 1651, 1353, 939, 1326, 445, 1223, 76986, 1023, 917, 1615, 1732, 1761, 367, 1078, 690, 1529, 1624, 997616, 1663, 1667, 928, 1449, 968, 1286, 72, 1621, 1622, 1643, 472, 1799, 1514, 1525, 1114, 1584, 1647, 1555, 1482, 1489, 1443, 1444, 1072, 1954, 1704, 1232, 1266, 1089, 1259, 1787, 1910, 1714, 1159, 1133, 1135, 1512, 892, 1084, 1031, 1067, 2936, 1411, 1271, 1807, 871, 1805, 1354, 1430, 8198, 1869, 634919, 485, 1594, 467, 1551, 390, 912, 913, 8091, 1471, 1474, 1446, 1092, 1718, 833, 1491, 1738, 1749, 1637, 1255, 1462, 1132, 1463, 1633, 1374, 1675, 691, 292, 1751, 1802, 1593, 1105, 1107, 1108, 1702, 1277, 1684, 1568, 1569, 1570, 1743, 1109, 1620, 1726, 639, 797, 1377, 1065, 4.5161E+15, 1708, 1709, 1328, 1592, 1121, 1295, 1104, 1064, 1063,

code_info

Catalog numbers: (1) 722003, (2) 722010, (3) 722026; UDI-DI: (1) No UDI, (2) 00884838059030, (3) 00884838054189; Serial…

Catalog numbers: (1) 722003, (2) 722010, (3) 722026; UDI-DI: (1) No UDI, (2) 00884838059030, (3) 00884838054189; Serial Numbers: (1) 285, 1634, 1349, 1153, 1154, 1472, 803, 1694, 1599, 1460, 1138, 1532, 940, 1214, 1627, 1728, 1189, 1311, 1700, 1187, 1222, 1651, 1353, 939, 1326, 445, 1223, 76986, 1023, 917, 1615, 1732, 1761, 367, 1078, 690, 1529, 1624, 997616, 1663, 1667, 928, 1449, 968, 1286, 72, 1621, 1622, 1643, 472, 1799, 1514, 1525, 1114, 1584, 1647, 1555, 1482, 1489, 1443, 1444, 1072, 1954, 1704, 1232, 1266, 1089, 1259, 1787, 1910, 1714, 1159, 1133, 1135, 1512, 892, 1084, 1031, 1067, 2936, 1411, 1271, 1807, 871, 1805, 1354, 1430, 8198, 1869, 634919, 485, 1594, 467, 1551, 390, 912, 913, 8091, 1471, 1474, 1446, 1092, 1718, 833, 1491, 1738, 1749, 1637, 1255, 1462, 1132, 1463, 1633, 1374, 1675, 691, 292, 1751, 1802, 1593, 1105, 1107, 1108, 1702, 1277, 1684, 1568, 1569, 1570, 1743, 1109, 1620, 1726, 639, 797, 1377, 1065, 4.5161E+15, 1708, 1709, 1328, 1592, 1121, 1295, 1104, 1064, 1063,

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1142-2025%22

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