FDA Device recall Z-1948-2024
HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100064…
- FDA Device
- Class II
- ongoing
- Published 2024-06-12
On 2024-06-12 the FDA classified a Class II recall of HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 9897100064… by Philips North America, citing oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1948-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-05-03 |
| Published | 2024-06-12 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006411
Reason
Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard
Identifiers
| code_info | UDI: N/A Serial Numbers: 3 5 6 9 11 12 13 14 15 16 17 18 19 20 22 23 25 26 29 30 31 32 33 34 35 37 38 39 41 42 43 44 45…UDI: N/A Serial Numbers: 3 5 6 9 11 12 13 14 15 16 17 18 19 20 22 23 25 26 29 30 31 32 33 34 35 37 38 39 41 42 43 44 45 49 50 51 52 53 55 56 58 61 63 64 66 67 68 70 71 72 73 75 77 79 80 81 82 83 84 86 87 88 89 91 93 94 95 97 98 100 101 102 103 104 105 107 108 109 110 111 112 113 114 115 116 117 118 119 120 122 123 124 125 126 129 130 132 133 135 136 137 138 139 140 141 142 143 146 148 149 150 151 152 153 154 155 156 158 159 160 161 162 163 164 165 167 169 170 171 172 173 174 175 177 180 181 183 184 185 186 188 189 190 191 192 193 195 196 197 198 200 201 202 203 204 205 206 207 208 209 211 212 213 215 216 218 219 220 221 222 223 224 225 226 228 229 232 233 234 235 236 237 238 240 241 242 243 244 246 248 250 251 253 254 255 257 258 259 260 262 263 264 265 267 269 270 272 273 274 275 278 279 281 282 284 286 287 288 289 290 291 292 293 294 295 296 297 298 301 302 303 304 305 307 308 309 310 311 312 313 314 315 317 318 319 320 322 323 324 325 326 328 331 332 334 335 336 337 338 339 340 341 |
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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-1948-2024%22
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