Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K041577 |
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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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Pinnacle3 Software Version 10.0, Model 459800200841. Product Usage: The Pinnacle 3 RTP software... | 2 | 05/21/2015 | Philips Medical Systems, Inc. |
Pinnacle3 Software Version 9.0, 9.2, 9.4 and 9.6, Model Numbers 453560446041, 459800091001, 459800... | 2 | 07/22/2015 | Philips Electronics North America Corporation |
Pinnacle3 Radiation Therapy Planning (RTP) System, software version 9.0. | 2 | 03/31/2014 | Philips Medical Systems (Cleveland), Inc. |
Pinnacle3 Radiation Therapy Planning System, software version 9.0. Model # Descriptio... | 2 | 01/11/2012 | Philips Medical Systems (Cleveland), Inc. |
Pinnacle3 VCC P/N 4598 001 41341 REV A, Philips Medical Systems (Cleveland), Inc., Fitchburg, WI. ... | 2 | 11/05/2012 | Philips Medical Systems (Cleveland), Inc. |
The Pinnacle3 Radiation Therapy Planning (RTP) system and its associated software; composed of seve... | 2 | 09/25/2007 | Philips Nuclear Medicine, Inc. |
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