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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K031552
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Product Description
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Recall
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FDA Recall
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Philips Diagnostic Ultrasound System, Model HD3. Product labeled HD3 Ultrasound System, Distributed... 2 12/31/2008 Philips Medical Systems
Philips Diagnostic Ultrasound System, Model HDI4000. Product labeled HDI4000 Ultrasound System, Dis... 2 12/31/2008 Philips Medical Systems
Biopsy Guide Starter Kits C7-3 used with the Philips HD3 Ultrasound System intended for diagnostic u... 2 09/16/2008 Philips Medical Systems
Biopsy Guide Starter Kits C5-2 used with the Philips HD3 Ultrasound System intended for diagnostic u... 2 09/16/2008 Philips Medical Systems
Biopsy Guide Starter Kits L9-5 used with the Philips HD3 Ultrasound System intended for diagnostic u... 2 09/16/2008 Philips Medical Systems
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