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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 126 Results
510(K) Number: K033326
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FDA Recall
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Ingenuity Core Model Number 728321 Product Usage: Computed Tomography X-ray systems intended to pr... 2 10/04/2016 Philips Medical Systems
Ingenuity Core 128 Model Number 728323 Product Usage: Computed Tomography X-ray systems intended... 2 10/04/2016 Philips Medical Systems
Ingenuity CT Model Number 728326 Product Usage: Computed Tomography X-ray systems intended to pr... 2 10/04/2016 Philips Medical Systems
Brilliance 64, 728231 Product Usage: Computed Tomography X-ray systems intended to produce cross... 2 04/13/2019 Philips Medical Systems (Cleveland) Inc
Brilliance 64, Model 728231 Product Usage: Computed Tomography X-ray systems intended to produc... 2 11/30/2018 Philips Medical Systems (Cleveland) Inc
Brilliance 40, Model 728235 Product Usage: Computed Tomography X-ray systems intended to produce... 2 11/30/2018 Philips Medical Systems (Cleveland) Inc
Brilliance 64 with DEPMED HARDENING KIT 12NC: 459800191351, Model Number 728231. Computed Tomography... 2 06/12/2018 Philips Medical Systems (Cleveland) Inc
Ingenuity Core - Model no. 728321, Computed Tomography X-Ray system Product Usage: Computed Tomogr... 2 04/17/2018 Philips Medical Systems (Cleveland) Inc
Brilliance 64 - Model no. 728231, Computed Tomography X-Ray system Product Usage: Computed Tomog... 2 04/17/2018 Philips Medical Systems (Cleveland) Inc
Ingenuity Core 128 - Model no. 728323, 728324, Computed Tomography X-Ray system Product Usage: C... 2 04/17/2018 Philips Medical Systems (Cleveland) Inc
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