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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 28 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-2851-2018 - DigitalDiagnost 4 High Performance (Stitching Patient Support) 712027 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2852-2018 - DigitalDiagnost 4.1 (Stitching Patient Support) 712225 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2853-2018 - DigitalDiagnost 4.1 Chest / Emergency (Stitching Patient Support) 712029 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2854-2018 - DigitalDiagnost 4.1 Flex / Value (Stitching Patient Support) 712028 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2855-2018 - DigitalDiagnost 4.1 High Performance (Stitching Patient Support) 712031 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2856-2018 - DigitalDiagnost Classic 1.x Upgrades (Stitching Patient Support) 712081 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2857-2018 - DigitalDiagnost Classic, Dual-Detector (Stitching Patient Support) 712052 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2858-2018 - DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2859-2018 - DigitalDiagnost Dual Detector (Stitching Patient Support) 712022 2 08/17/2018 Philips Medical Systems Gmbh, DMC
Z-2860-2018 - DigitalDiagnost Rel.4 Upgrades (Stitching Patient Support) 712084 2 08/17/2018 Philips Medical Systems Gmbh, DMC
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