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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 16 Results
Related Medical Device Recalls Recall Date to: 11/22/2014
 
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Product Description
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FDA Recall
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Z-0133-2009 - ANGIOSTAR X-Ray System, Model numbers 9359142 and 6379668. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0148-2009 - NEUROSTAR TOP X-Ray System, Model numbers 6258425 and 6379668. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0135-2009 - MULTISTAR D X-Ray System, Model number 3772501. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0136-2009 - Coroskop X-Ray System, Model numbers 6258219 and 6379759. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0137-2009 - Bicor X-Ray System, Model number 9023136. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0138-2009 - Bicor Hi-P X-Ray System, Model numbers 6379767 and 6258383. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0139-2009 - MULTISTAR P X-Ray System, Model number 3773004. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0140-2009 - Coroskop Top X-Ray System, Model number 6134808. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0141-2009 - Coroskop C X-Ray System, Model numbers 6005636 and 9108572. 2 11/04/2008 Siemens Medical Solutions USA, Inc
Z-0142-2009 - MULTISTAR POLYDOROS X-Ray System, Model number 2845001 2 11/04/2008 Siemens Medical Solutions USA, Inc
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