FDA Device recall Z-1144-2025

Allura Xper FD20

FDA Device
Class I
ongoing
Published 2025-02-26

On 2025-02-26 the FDA classified a Class I recall of Allura Xper FD20 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-1144-2025
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 FD20; Catalog numbers: (1) 722006, (2) 722012, (3) 722028.

Reason

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

Identifiers

code_info	Catalog numbers: (1) 722006, (2) 722012, (3) 722028; UDI-DI: (1) No UDI, (2) 00884838059054, (3) 00884838054202; Serial… Catalog numbers: (1) 722006, (2) 722012, (3) 722028; UDI-DI: (1) No UDI, (2) 00884838059054, (3) 00884838054202; Serial Numbers: (1) 2013, 2155, 1473, 2110, 1364, 2268, 172, 2324, 1637, 1881, 2229, 2533, 2158, 1774, 468, 813, 1477, 2051, 2462, 1352, 2562, 771, 1734, 1589, 1445, 1547, 929, 1414, 731, 2131, 635249, 2569, 1461, 914, 2097, 1890, 2281, 1896, 1762, 1764, 159, 774, 2198, 2009, 1629, 810, 1729, 2454, 1209, 1646, 1924, 1339, 2301, 1927, 1928, 1706, 1705, 2571, 2524, 1582, 972, 878, 2200, 1575, 707, 1761, 861, 2537, 722, 72246F, 1674122, 1730, 1936, 1490, 2045, 2536, 1338, 1659, 2610, 920, 1662, 1346, 1587, 1977, 2140, 664, 706, 1843, 1594, 1875, CV.381, 886, 2523, 2267, 2823014, 1583, 1585, 1520, 2126, 1856, 1941, 288, 2390, 1425, 1496, 862, 896, 2608, 1393, 2204, 2366, 2449, 2456, 2269, 2425, 2066, 1744, 1747, 1748, 1325, 1812, 2606, 641, 1728, 559, 1443, 2530, CV.271, 283, 1755, 1120, 889, 518, 1007, 1104, 1914, 1752, 2565, 848, 904, 1754, 1375, 1696, 843, 2021, 2195, 1723, 7

code_info

Catalog numbers: (1) 722006, (2) 722012, (3) 722028; UDI-DI: (1) No UDI, (2) 00884838059054, (3) 00884838054202; Serial…

Catalog numbers: (1) 722006, (2) 722012, (3) 722028; UDI-DI: (1) No UDI, (2) 00884838059054, (3) 00884838054202; Serial Numbers: (1) 2013, 2155, 1473, 2110, 1364, 2268, 172, 2324, 1637, 1881, 2229, 2533, 2158, 1774, 468, 813, 1477, 2051, 2462, 1352, 2562, 771, 1734, 1589, 1445, 1547, 929, 1414, 731, 2131, 635249, 2569, 1461, 914, 2097, 1890, 2281, 1896, 1762, 1764, 159, 774, 2198, 2009, 1629, 810, 1729, 2454, 1209, 1646, 1924, 1339, 2301, 1927, 1928, 1706, 1705, 2571, 2524, 1582, 972, 878, 2200, 1575, 707, 1761, 861, 2537, 722, 72246F, 1674122, 1730, 1936, 1490, 2045, 2536, 1338, 1659, 2610, 920, 1662, 1346, 1587, 1977, 2140, 664, 706, 1843, 1594, 1875, CV.381, 886, 2523, 2267, 2823014, 1583, 1585, 1520, 2126, 1856, 1941, 288, 2390, 1425, 1496, 862, 896, 2608, 1393, 2204, 2366, 2449, 2456, 2269, 2425, 2066, 1744, 1747, 1748, 1325, 1812, 2606, 641, 1728, 559, 1443, 2530, CV.271, 283, 1755, 1120, 889, 518, 1007, 1104, 1914, 1752, 2565, 848, 904, 1754, 1375, 1696, 843, 2021, 2195, 1723, 7

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-1144-2025%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.