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FDA (Device enforcement)Recalled 2024-05-03class ii

Philips North America Llc: HA FlexTrak-Patient transport functionality to transport the patient from the preparation area to the MR system, Product Number: 989710006411

Hazard

Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard

Details from the source

Reason for recall: Oil may leak from the HA FlexTrack Trolley onto the floor when pressing the hydraulic pedal, resulting in a potential slipping/falling hazard Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, Bangladesh, Belgium, Brazil, Canada, Chile, China, Colombia, Czech Republic, Denmark, Estonia, Fiji, Finland, France, French Guiana, Germany, Guadeloupe, Honduras, Hong Kong, India, Indonesia, Ireland, Italy, Japan, Jordan, Lithuania, Martinique, Mexico, Morocco, Netherlands, Norway, Oman, Peru, Poland, Russia Quantity: 1348 units Lot/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 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 98 100 101 102 103 104 105 107 108 109 110 111 112 113 114 115 116 117 118 119 120 122 123 124 125 126 129 130 132 133 135 136 137 138 139 140 141 142 143 146 148 149 150 151 152 153 154 155 156 158 159 160 161 162 163 164 165 167 169 170 171 172 173 174 175 177 180 181 183 184 185 186 188 189 190 191 192 193 195 196 197 198 200 201 202 203 204 205 206 207 208 209 211 212 213 215 216 218 219 220 221 222 223 224 225 226 228 229 232 233 234 235 236 237 238 240 241 242 243 244 246 248 250 251 253 254 255 257 258 259 260 262 263 264 265 267 269 270 272 273 274 275 278 279 281 282 284 286 287 288 289 290 291 292 293 294 295 296 297 298 301 302 303 304 305 307 308 309 310 311 312 313 314 315 317 318 319 320 322 323 324 325 326 328 331 332 334 335 336 337 338 339 340 341 342 343 344 345 346 347 350 351 352 355 356 358 359 360 361 362 363 364 366 367 368 369 370 371 372 373 374 375 379 380 381 382 384 386 387 388 390 391 392 394 395 396 397 399 400 401 402 403 404 405 406 408 409 411 412 413 414 415 416 417 419 420 421 422 423 424 426 427 428 429 431 432 434 435 436 437 438 439 440 441 442 444 445 446 448 449 450 451 452 453 454 456 457 460 461 462 463 464 465 466 467 468 469 472 473 474 475 476 477 478 479 480 481 482 483 485 487 489 491 492 493 494 496 497 498

Source

Official record: FDA (Device enforcement)

Republished from the official source above; details can change — the source record controls.

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