Reported Dec 19, 2012 · Terminated

MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light

Siemens Medical Solutions USA, 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: Siemens Medical Solutions USA, Inc · 51 Valley Stream Pkwy · Malvern, PA · 19355

Is this the product you have?

  • MAVIG PORTEGRA 2 system operated in conjuction with a Siemens AX system Ceiling mounted surgical light
Lot codes and dates
    • Part numbers 7721165
    • 4787714
    • 7559375
    • 10281150
    • 10281151
    • 10281152 and 10281183
Amount recalled
1315

Where it was sold

  • Nationwide

Why it was recalled

A particular component may not have been fitted during the installation of some MAVIG PORTEGRA 2 systems.

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 Nov 6, 2014 · Data as of Sep 19, 4:53 PM UTC

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