Reported Jan 3, 2018 · Terminated

TomoHD(R) System, Model Number 1018283 Product Usage: The TomoTherapy treatment system is intended to be used as an…

Accuray Incorporated

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

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Accuray Incorporated · 1240 Deming Way · Madison, WI · 53717-1954

Is this the product you have?

  • TomoHD(R) System
  • Model Number 1018283 Product UsageThe 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
Lot codes and dates
  • Serial Numbers

    118 of 118 codes

    • 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
Amount recalled
118 units

This recall covers 4 products

The agency filed one notice per product. You are reading one of them; the other 3 are below.

Why it was recalled

Uncontrolled couch Z-axis movement (descent)

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

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Jul 25, 2021 · Data as of Sep 19, 4:49 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.