Reported Mar 25, 2015 · Terminated

Elekta Precise Treatment Table

Elekta, Inc.

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: Elekta, Inc. · 400 Perimeter Center Ter Ne · Atlanta, GA · 30346-1227

Is this the product you have?

  • Elekta Precise Treatment Table
Lot codes and dates
  • Precise Treatment Table Serial Numbers
    • (124001-125803
    • 125807-880
    • 125883-899
    • 125902-917
    • 125920-949
    • 125952-963
    • 125966-1256453
    • 126158-170
    • 126174-208
    • 126212-230
    • 126232-261
    • 126269-281
    • 126293-309
    • 123318-330
    • 126338-126373
    • 126375-397
    • 126400-133999
    • 213000+)
Amount recalled
529 US 2951 Worldwide

Where it was sold

  • Nationwide

Why it was recalled

It is possible to position the Treatment Table with errors greater than 5mm and no inhibits are displayed, if the positional sensors are not correctly installed during corrective maintenance. Clinical mistreatment may occur if a position error is not detected.

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

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Elekta, Inc. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

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

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 5, 2021 · Data as of Sep 19, 5:31 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.