Medical Device Recalls
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1 to 10 of 500 Results
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Recall Date to: 09/12/2015 Firm: Philips Medical Systems |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Intellivue Information Center Model: M3150BU#CO1 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Intellivue Information Center Model: M3150B#C01 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Viridia/Agilent Information Center Model : M3151A#CO1 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Viridia/Agilent Information Center Model : M3150A#C01 | 2 | 02/28/2003 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Philips HeartStart XL, Model M4735A Defibrillator/Monitor | 2 | 12/18/2002 | Philips Medical Systems, Inc. Cardiac & Monitoring Systems |
Pinnacle3 Software Version 10.0, Model 459800200841. Product Usage: The Pinnacle 3 RTP software... | 2 | 05/21/2015 | Philips Medical Systems, Inc. |
Philips Healthcare DuraDiagnost X- Ray | 2 | 05/19/2015 | Philips Medical Systems, Inc. |
Philips Healthcare DigitalDiagnost System X-Ray | 2 | 05/19/2015 | Philips Medical Systems, Inc. |
Lithium Polymer Fiber Optic Module Batteries used in the Intera MR System upgraded to CDAS, Part Num... | 2 | 03/20/2015 | Philips Medical Systems, Inc. |
Philips DuraDiagnost X-Ray system, Stationary X-Ray System Radiographic Models: 712210, 712211 | 2 | 03/06/2015 | Philips Medical Systems, Inc. |
* The maximium 500 devices meeting your search criteria returned. Please narrow your search. |
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