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Recall Observatory FDA recall evidence

Exact FDA event identifier

Event 78686

4 recalled-product records grouped only because every row carries this exact official event ID.

Open FDA event record

Event summary

Timeline bucket
November 17, 2017
Product types
Device
Classifications
Class II
Statuses
Terminated
Recalling firm wording
Accuray Incorporated

Dossier provenance

Source snapshots represented here

  • openFDA Device Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.
  • openFDA Device Recall event_date_initiated coverage June 01, 1997–June 30, 2026

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Complete imported group

Every recalled product in this event

4 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

device · product 1 of 4

Hi-Art(R) System, Model Number H-000-0003 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional conformal) format in accordance with the physicians prescribed and approved plan.

Z-0286-2018
Recall number
Z-0286-2018
Initiated
November 17, 2017
Classification
Class II
Status
Terminated
Recalling firm
Accuray Incorporated
Quantity
250 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Uncontrolled couch Z-axis movement (descent)

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Uncontrolled couch Z-axis movement (descent)

Code information

Serial Numbers: 110016 110022 110024 110029 110030 110036 110038 110045 110046 110050 110054 110055 110056 110058 110060 110061 110065 110066 110067 110069 110071 110073 110077 110078 110084 110085 110087 110088 110090 110091 110092 110094 110097 110098 110099 110103 110104 110106 110109 110110 110112 110113 110114 110115 110116 110117 110120 110122 110124 110125 110126 110127 110128 110133 110136 110141 110142 110144 110146 110148 110150 110151 110152 110153 110154 110156 110157 110159 110161 110164 110165 110166 110167 110168 110170 110171 110172 110174 110175 110176 110177 110181 110183 110184 110189 110190 110191 110192 110193 110196 110198 110200 110202 110203 110204 110205 110207 110209 110210 110211 110212 110213 110215 110216 110217 110218 110220 110222 110223 110224 110225 110227 110229 110232 110233 110234 110235 110236 110238 110239 110240 110241 110244 110245 110246 110247 110249 110251 110252 110253 110254 110255 110256 110257 110258 110259 110260 110261 110262 110263 110267 110269 110271 110272 110273 110275 110276 110278 110279 110281 110282 110283 110284 110285 110287 110288 110291 110292 110293 110294 110295 110296 110297 110298 110299 110301 110303 110304 110305 110306 110307 110308 110310 110312 110313 110314 110316 110317 110319 110320 110321 110323 110324 110325 110326 110327 110328 110329 110330 110331 110334 110335 110337 110339 110340 110341 110342 110343 110344 110345 110346 110349 110351 110356 110358 110359 110361 110362 110365 110366 110367 110370 110371 110372 110374 110375 110377 110382 110383 110389 110393 110395 110400 110403 110404 110416 110421 110423 110428 110429 110432 110433 110435 110438 110439 110440 110443 110449 110450 110456 110459 110468 110497 110499 110505 110507 110508 110509 110510 110522

Distribution pattern

Worldwide Distribution

device · product 2 of 4

TomoHD(R) System, Model Number 1018283 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional conformal) format in accordance with the physicians prescribed and approved plan.

Z-0287-2018
Recall number
Z-0287-2018
Initiated
November 17, 2017
Classification
Class II
Status
Terminated
Recalling firm
Accuray Incorporated
Quantity
118 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Uncontrolled couch Z-axis movement (descent)

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Uncontrolled couch Z-axis movement (descent)

Code information

Serial Numbers: 110081 110100 110158 110180 110185 110194 110197 110208 110214 110228 110265 110266 110268 110286 110300 110311 110315 110332 110333 110347 110350 110354 110355 110357 110363 110368 110376 110378 110379 110380 110381 110385 110386 110387 110388 110390 110391 110392 110394 110396 110397 110401 110402 110405 110406 110407 110409 110412 110413 110414 110415 110419 110420 110422 110425 110426 110427 110430 110431 110434 110436 110437 110441 110442 110444 110445 110446 110447 110448 110451 110453 110454 110455 110458 110460 110464 110465 110466 110467 110469 110471 110472 110480 110482 110501 110504 110506 110511 110512 110517 110527 110528 110531 110532 110534 110539 110540 110541 110544 110545 110546 110547 110548 110549 110553 110555 110558 110563 110566 110569 110574 110578 110579 110591 110594 110596 110597 110606

Distribution pattern

Worldwide Distribution

device · product 3 of 4

TomoH(R) System, Model Number 1018284 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional conformal) format in accordance with the physicians prescribed and approved plan.

Z-0288-2018
Recall number
Z-0288-2018
Initiated
November 17, 2017
Classification
Class II
Status
Terminated
Recalling firm
Accuray Incorporated
Quantity
29 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Uncontrolled couch Z-axis movement (descent)

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Uncontrolled couch Z-axis movement (descent)

Code information

Serial Numbers: 110040 110083 110163 110231 110237 110289 110302 110369 110418 110461 110462 110474 110491 110494 110503 110519 110525 110533 110536 110537 110552 110554 110556 110562 110565 110570 110573 110576 110577

Distribution pattern

Worldwide Distribution

device · product 4 of 4

TomoHDA(R) System, Model Number 1018286 Product Usage: The TomoTherapy treatment system is intended to be used as an integrated system for t he planning and precise delivery of radiation therapy, stereotactic radiotherapy, or stereotactic radiosurgery to tumors or other targeted tissues while minimizing the delivery of radiation to vital healthy tissues. The megavoltage x-ray radiation is delivered in a rotational, non-rotational, modulated (IMRT), or non- modulated (non-IMRT/3 dimensional conformal) format in accordance with the physicians prescribed and approved plan.

Z-0289-2018
Recall number
Z-0289-2018
Initiated
November 17, 2017
Classification
Class II
Status
Terminated
Recalling firm
Accuray Incorporated
Quantity
87 units

App-derived interpretation

Unknown reason.no_named_rule · v1.0.0
Uncontrolled couch Z-axis movement (descent)

These labels are deterministic app interpretations, not FDA categories.

Official device-enrichment evidence · Sourced

Software design

Compare all device evidence states

Inspect official wording and provenance

Reason for recall

Uncontrolled couch Z-axis movement (descent)

Code information

Serial Numbers: 110033 110137 110155 110206 110221 110290 110318 110348 110353 110360 110364 110384 110408 110410 110411 110452 110457 110463 110473 110475 110476 110477 110478 110479 110481 110483 110484 110485 110486 110487 110488 110489 110490 110492 110493 110496 110498 110500 110502 110513 110514 110515 110516 110518 110520 110521 110523 110524 110526 110529 110530 110535 110538 110542 110543 110550 110551 110557 110559 110560 110561 110564 110567 110571 110572 110575 110580 110582 110583 110584 110585 110586 110587 110588 110593 110598 110599 110600 110603 110604 110605 110609 110610 110612 110613 110614 110616

Distribution pattern

Worldwide Distribution

Field note

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