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FDASeptember 24, 2014device

Foot Switches used with the following systems: Philips Allura Xper Systems; 722001 AlluraXperFDlO C, 722002 Allura Xper FD1O F, 722003 Allura Xper FD1O, 722005 Allura Xper FD1O/10, 722006 Allura Xper FD2O, 722008 Allura Xper FD2O Biplane, 722010 Allura Xper FD1O, 722011 Allura Xper FD1O/10, 72201...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Loss of key image functionality due to a bent pedal of the Footswitch.

What to do

FDA enforcement status: Terminated

Brands named

philips medical systemsphilipsphilips medical

UPCs

452270000141452270000151452270000142452270000381452270000382459800076001459800076021459800415571459800415581459800415531459800415561

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Foot Switches used with the following systems: Philips Allura Xper Systems; 722001 AlluraXperFDlO C, 722002 Allura Xper FD1O F, 722003 Allura Xper FD1O, 722005 Allura Xper FD1O/10, 722006 Allura Xper FD2O, 722008 Allura Xper FD2O Biplane, 722010 Allura Xper FD1O, 722011 Allura Xper FD1O/10, 72201... — Recall Details · AllClear