Reported Feb 3, 2016 · Terminated

Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray…

Midmark Corp. dba Progeny 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: Midmark Corp dba Progeny Inc · 675 Heathrow Dr · Lincolnshire, IL · 60069-4206

Is this the product you have?

  • Vantage Panoramic X-Ray System used to perform dental and orthodontic radiological imaging The Vantage Panoramic X-Ray System is a class II extra oral X-Ray system used to provide dental radiographic examination and diagnosis of diseases of the teeth, jaw and oral structures. When the system is equipped with the cephalometric option, the system will also provide cephalometric radiographic examinations for use in orthodontic treatment planning and evalu
Lot codes and dates
  • Model Number

    832 of 832 codes

    • 60-A0001
    • ZA05002
    • ZA05003
    • ZA05004
    • ZA05005
    • ZA05006
    • ZA05007
    • ZA05008
    • ZA05009
    • ZA05010
    • ZA05011
    • ZA05012
    • ZA05013
    • ZA05014
    • ZA05015
    • ZA05016
    • ZA05017
    • ZA05018
    • ZA05019
    • ZA05020
    • ZA05021
    • ZA05022
    • ZA05023
    • ZB51001
    • ZB51002
    • ZB51003
    • ZB51004
    • ZB51007
    • ZB51008
    • ZB51009
    • ZB51010
    • ZB51011
    • ZB51012
    • ZB51013
    • ZB51014
    • ZB51015
    • ZB51016
    • ZB51017
    • ZB51018
    • ZB51019
    • ZB51021
    • ZB51023
    • ZB51024
    • ZB51025
    • ZB51026
    • ZB51027
    • ZB51028
    • ZB51029
    • ZB51030
    • ZB51031
    • ZB51032
    • ZB51034
    • ZB51035
    • ZB51036
    • ZB52001
    • ZB52002
    • ZB52003
    • ZB52004
    • ZB52005
    • ZB52006
Amount recalled
832 systems

Where it was sold

Why it was recalled

Failure of the primary collimator may result in unintentional movement of the device. The unintentional movement will not result in the generation of an error message.

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 Midmark Corp. dba Progeny 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 Dec 29, 2017 · Data as of Sep 19, 5:21 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.