Medical Device Recalls
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1 to 5 of 5 Results
Recall Date to: 01/31/2015 510(K) Number: K132304 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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EPIQ 7 Ultrasound System, EPIQ 7 systems with software versions 1.0.x or 1.1.x with QLAB a2DQ and/or... | 2 | 12/16/2014 | Philips Ultrasound, Inc. |
EPIQ 5 Ultrasound System, EPIQ 5 systems with software versions 1.0.x or 1.1.x with QLAB a2DQ and/or... | 2 | 12/16/2014 | Philips Ultrasound, Inc. |
Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow a... | 2 | 03/20/2014 | Philips Medical Systems North America Inc. |
Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound imaging and fluid flow a... | 2 | 03/20/2014 | Philips Medical Systems North America Inc. |
EPIQ 7 Ultrasound System, Model 795200, 795201, 795202. Intended for diagnostic ultrasound imagin... | 2 | 11/20/2013 | Philips Medical Systems North America Inc. |
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