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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 24 Results
Related Medical Device Recalls
 
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0744-2011 - HiSpeed LXI (2200997) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0788-2011 - HiSpeed FX/I (2201000-2 with Gantry mo. #2249696-2) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0746-2011 - HiSpeed DX/I (2201000) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0747-2011 - HiSpeed DX/I (2201000-2) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0768-2011 - HiSpeed DX/I (2249696) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0770-2011 - Hi Speed DX/I (2249696-2) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0771-2011 - HiSpeed FX/I (2200997 with Gantry mo. #2200997) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0772-2011 - HiSpeed FX/I (2200997 with Gantry mo. #2201000) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0773-2011 - HiSpeed FX/I (2200997 with Gantry mo. #2200997-2) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
Z-0774-2011 - HiSpeed FX/I (2200997 with Gantry mo. #2201000-2) 2 01/04/2011 FEI # 2126677
GE Healthcare, LLC
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