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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Diagnostic Equipment

Philips Allura Xper Systems Recalled for Motorized Movement Failure

Agency Publication Date: September 25, 2025
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Summary

Philips Medical Systems is recalling 4,234 Allura Xper medical imaging systems because internal parts like batteries, hard drives, and power supplies can wear out and fail. If these components deteriorate, the system's motorized movements—which are used to position the equipment around a patient—may stop working during a procedure. While automated movements might fail, manual movements of the stand and table remain functional, and the X-ray imaging capabilities are not affected. Philips has initiated this voluntary recall to address the deterioration of these internal components.

Risk

A failure of motorized movements during a medical procedure can prevent the precise positioning of imaging equipment, potentially leading to delays in treatment or the need to manually reposition the system. While manual overrides are available, a sudden loss of automated control could complicate time-sensitive medical interventions.

What You Should Do

  1. The recalled products are various Philips Allura Xper systems including FD10, FD20, and Biplane models used in clinical settings.
  2. Check the model name and serial number on your system's identification label to see if your device is affected. See the Affected Products section below for the full list of affected codes.
  3. Stop using the recalled device and contact Philips Medical Systems or your authorized distributor to arrange for a service technician to inspect and correct the system components.
  4. Call the FDA's Center for Devices and Radiological Health (CDRH) at 1-888-463-6332 if you have additional questions or wish to report a concern.

Your Remedy Options

📋Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: Allura Xper FD10
Model / REF:
722010
722026
722003
Serial Numbers (916):
764
177
662
905
480
499
833
787
1336
839
1048
343
1011
917
108
671
677
468
1132
1025
1226
411
1108
1043
1302
160
1309
638
527
1442
1109
679
467
986
1112
968
505
286
636
946
214
755
1365
809
763
992
521
647
1176
67
UDI:
00884838059030
00884838054189

Quantity: 1117 units (252 US, 865 OUS). Recall #: Z-2623-2025.

Product: Allura Xper FD10/10
Model / REF:
722011
722027
722005
Serial Numbers (237):
157
268
95
107
59
319
49
170
173
101
84
155
133
234
345
332
102
270
177
132
325
15
87
255
171
362
168
275
344
324
163
103
215
328
286
81
293
294
224
117
334
338
146
145
266
21
202
165
367
372
UDI:
00884838059047
00884838054196

Quantity: 286 units (67 US, 219 OUS). Recall #: Z-2624-2025.

Product: Allura Xper FD10 OR Table
Model / REF:
722022
722033
Serial Numbers:
6
1
UDI:
00884838059078
00884838054233

Quantity: 2 units (1 US, 1 OUS). Recall #: Z-2625-2025.

Product: Allura Xper FD20
Model / REF:
722012
722028
722006
Serial Numbers (1724):
919
1581
1117
1001
1673
1712
585
517
1545
1715
504
757
935
1356
1250
1613
2006
1440
1550
1733
1734
2201
1922
741
2283
1034
1359
1848
950
2943
865
1908
1166
1113
1804
100
1408
590
2508
1279
2509
452
2151
1724
2134
481
543
893
1455
2085
UDI:
00884838059054
00884838054202

Quantity: 2114 units (791 US, 1323 OUS). Recall #: Z-2626-2025.

Product: Allura Xper FD20 Biplane
Model / REF:
722013
722008
Serial Numbers (253):
505
313
34
153
410
360
290
241
404
126
244
106
346
383
461
307
442
435
293
289
267
214
402
86
603
149
424
140
254
255
266
518
519
303
115
150
129
496
441
124
151
550
575
562
178
330
309
601
308
264
UDI:
00884838059061

Quantity: 268 units (102 US, 166 OUS). Recall #: Z-2627-2025.

Product: Allura Xper FD20 OR Table
Model / REF:
722023
722035
722015
Serial Numbers (128):
27
116
12
175
98
35
142
179
46
64
110
124
66
117
109
42
138
82
83
127
75
118
41
121
70
119
112
25
159
137
47
173
114
167
164
4
16
14
107
9
13
105
5
132
2
21
38
102
52
84
UDI:
00884838059085
00884838054240

Quantity: 174 units (45 US, 129 OUS). Recall #: Z-2628-2025.

Product: Allura Xper FD20 Biplane OR Table
Model / REF:
722020
722025
Serial Numbers:
6
4
2
3
UDI:
00884838059108

Quantity: 5 units (2 US, 3 OUS). Recall #: Z-2629-2025.

Product: Allura Xper FD20/20
Model / REF:
722038
Serial Numbers (75):
39
63
42
55
67
99
60
71
115
78
106
118
130
49
119
126
173
37
38
48
62
35
137
131
70
46
102
122
121
113
152
111
138
14
127
94
93
132
92
89
88
66
30
58
29
170
28
47
104
112
Lot Numbers:
722038
UDI:
00884838054226

Quantity: 75 units (26 US, 49 OUS). Recall #: Z-2630-2025.

Product: Allura Xper FD20/20 OR Table
Model / REF:
722039
Serial Numbers:
2
4
5
Lot Numbers:
722039
UDI:
00884838054271

Quantity: 3 units (OUS only). Recall #: Z-2631-2025.

Product: Allura Xper FD20/10
Model / REF:
722029
Serial Numbers:
71
7
62
36
21
30
63
129
56
57
31
24
32
39
69
34
45
37
23
44
40
38
75
35
61
53
25
58
85
27
46
19
14
20
52
70
78
29
59
49
50
81
80
47
43
Lot Numbers:
722029
UDI:
00884838054219

Quantity: 45 units (11 US, 34 OUS). Recall #: Z-2632-2025.

Product: Allura Xper FD20/15
Model / REF:
722058
Serial Numbers (98):
249
22
71
85
138
24
167
168
129
149
259
134
38
56
61
99
59
109
100
124
94
23
111
110
108
32
161
89
18
19
409
66
55
40
72
15
9
25
81
119
60
164
7
101
106
145
136
137
76
112
Lot Numbers:
722058
UDI:
00884838059115

Quantity: 98 units (23 US, 75 OUS). Recall #: Z-2633-2025.

Product: Allura Xper FD20/15 OR Table
Model / REF:
722059
Serial Numbers:
2
Lot Numbers:
722059
UDI:
00884838059122

Quantity: 1 units (OUS only). Recall #: Z-2634-2025.

Product: Allura CV20
Model / REF:
722031
Serial Numbers:
155
150
87
88
109
97
138
86
152
135
153
35
76
133
173
124
92
166
61
130
116
117
110
112
113
89
90
S01H000984
177
164
165
161
162
163
100
174
167
158
134
136
180
115
83
77
94
85
Lot Numbers:
722031

Quantity: 46 units (OUS only). Recall #: Z-2635-2025.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 97501
Status: Active
Manufacturer: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Sold By: Authorized Medical Device Distributors; Direct Hospital Sales
Manufactured In: Netherlands
Units Affected: 13 products (1117 units (252 US, 865 OUS); 286 units (67 US, 219 OUS); 2 units (1 US, 1 OUS); 2114 units (791 US, 1323 OUS); 268 units (102 US, 166 OUS); 174 units (45 US, 129 OUS); 5 units (2 US, 3 OUS); 75 units (26 US, 49 OUS); 3 units (OUS only); 45 units (11 US, 34 OUS); 98 units (23 US, 75 OUS); 1 units (OUS only); 46 units (OUS only))
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.