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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K141736
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FDA Recall
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digital x-ray detector ProGrade R1 - solid state X ray imager (flat panel/digital imager) As a... 2 02/23/2018 FEI # 1218950
Philips Electronics North America Corporation
Philips DigitalDiagnost 3.1.x X-Ray System 2 06/09/2017 FEI # 1218950
Philips Electronics North America Corporation
Philips DigitalDiagnost Release 4.0.3, Release 4.1/4.1.1. excluding systems with SP1 Product Us... 2 11/11/2015 FEI # 1218950
Philips Electronics North America Corporation
Philips Healthcare DigitalDiagnost stationary X-ray system 2 06/03/2016 FEI # 1218950
Philips Healthcare
Philips DigitalDiagnost software 4.1.x and 4.2.x, A Stationary X-ray System Models: 712027, 712028,... 2 10/24/2018 FEI # 3003768251
Philips Medical Systems Gmbh, DMC
Philips Healthcare DigitalDiagnost System X-Ray 2 05/19/2015 FEI # 1218950
Philips Medical Systems, Inc.
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