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  "name": "DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20",
  "description": "FDA recall Z-1913-2025 — Beckman Coulter, Inc. is recalling DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20 (Devices, Class II). The enforcement record is RECORDED; the classification is a DETERMINATION (FDA's regulatory verdict); the boundary is INTERPRETATION (a recall ≠ harm to a specific person). Source: openFDA. CC0.",
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      "name": "FDA recall Z-1913-2025: Beckman Coulter, Inc. is recalling DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20",
      "text": "The FDA logged enforcement record Z-1913-2025: Beckman Coulter, Inc. is voluntarily recalling DxI 9000 Access Immunoassay Analyzer, Catalog Number C11137, running software version 1.20 — reason: A new software update (v1.20) is introducing error codes for the Dxl 9000 which prevents the assay from being performed and a delay in results from being generated, and may require field service to resolve the delay.. Status: Ongoing — the recall is still being carried out.. Initiated 2025-04-23. Affected lots/codes: UDI-DI: 15099590732103; Serial Numbers: 300573 300572 300571 300570 300569 300568 300567 300566 300564 300563 300562 300561 300560 300559 300558 300557 300556 300555 300554 300553 300552 300551 300548 300547 300546 300544 300543 300542 300541 300540 300539 300538 300537 300536 300535 300534 300533 300532 300531 300530 300528 300527 300526 300525 300524 300523 300522 300521 300520 300519 300518 300517 300516 300515 300514 300512 300511 300510 300509 300508 300507 300506 300501 300500 300497 300496 300495 300493 300491 300490 300489 300481 300479 300476 300475 300474 300470 300468 300467 300464 300458 300457 300455 300446 300438 300434 300430 300428 300427 300426 300425 300424 300423 300422 300420 300415 300414 300413 300411 300410 300409 300408 300407 300403 300398 300397 300396 300395 300393 300392 300389 300388 300378 300376 300375 300373 300372 300370 300362 300361 300360 300359 300358 300356 300354 300352 300350 300346 300341 300339 300338 300336 300334 300333 300331 300329 300328 300327 300326 300323 300322 300319 300318 300317 300316 300314 300312 300309 300306 300300 300299 300293 300288 300286 300285 300284 300283 300282 300280 300279 300275 300274 300273 300272 300270 300267 300266 300255 300252 300250 300249 300242 300240 300236 300235 300234 300232 300231 300228 300226 300225 300221 300219 300218 300217 300215 300214 300213 300212 300211 300210 300209 300208 300206 300205 300204 300201 300200 300198 300194 300193 300192 300191 300190 300186 300183 300182 300178 300175 300174 300171 300168 300166 300161 300158 300157 300156 300155 300154 300153 300150 300148 300145 300144 300138 300136 300132 300128 300126 300124 300116. A RECORDED FDA enforcement action (occurred=true).",
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      "text": "A recall is a RECORDED FDA enforcement action — the FDA logged that a firm is removing or correcting a product, classed by the FDA's risk judgment. It does NOT establish that any specific unit is affected or caused harm; causation is not established. This record informs and compares — it is NOT medical advice and does not tell anyone to start or stop a drug or device. For a medical decision, route to the FDA recall record and a licensed pharmacist or prescriber.",
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