Is this the product you have?

Lot codes and dates: (1)
System Code722015
UDIN/A
System Serial Number
12
16
2
8
23
3
13
(2)
System Code722023
UDI00884838059085
System Serial Number
100 of 100 codes
49
41
142
110
12
179
124
27
98
66
118
117
138
42
64
116
127
175
75
82
83
46
35
109
146
33
165
169
101
103
129
10
105
90
107
100
47
159
137
119
164
70
95
177
158
5
86
34
132
9
108
121
31
112
173
114
170
172
4
14
System Code722035
UDI00884838054240
System Serial Number
190 of 190 codes
119
126
169
72
124
161
183
242
245
246
46
196
52
236
147
172
123
74
59
60
88
30
216
212
85
21
47
222
121
131
145
127
38
187
243
143
244
125
117
100
57
247
34
165
252
101
89
192
111
128
227
144
174
28
84
130
263
132
25
98
Amount recalled: 196 units (73 US, 223 OUS)

This recall covers 23 products

The agency filed one notice per product. You are reading one of them; the other 22 are below.

10 more are in the archive.

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

This product could cause temporary or reversible health problems — stop using it.

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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45 in total.