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U.S. Department of Health and Human Services

Medical Device Recalls
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91 to 100 of 103 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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Z-1990-2017 - Rotating Large Craniotome 2 05/04/2017 The Anspach Effort, Inc.
Z-2028-2017 - SMALL ATTACHMENT, J-LATCH 2 05/04/2017 The Anspach Effort, Inc.
Z-2027-2017 - SMALL ATTACHMENT, JACOBS CHUCK 2 05/04/2017 The Anspach Effort, Inc.
Z-1962-2017 - STANDARD CRANIOTOME, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
Z-2031-2017 - Sagittal MICRO-SAW 2 05/04/2017 The Anspach Effort, Inc.
Z-2015-2017 - Sagittal Saw Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1957-2017 - System Console, Single Port, no irrigation 2 05/04/2017 The Anspach Effort, Inc.
Z-1956-2017 - System Console, Single Port, with irrigation Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1944-2017 - XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1945-2017 - XMAX Motor, High Strength Hose Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
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