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U.S. Department of Health and Human Services

Medical Device Recalls

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71 to 80 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
Posting Date
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Recalling Firm
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Z-1953-2017 - Foot Control, SC2100 Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1933-2017 - Foot control irrigation system Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1963-2017 - GREEN ROTATING CRANIOTOME, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
Z-1942-2017 - IMRI AIR CONTROL Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1996-2017 - IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1943-2017 - IMRI MOTOR Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1997-2017 - IMRI SHORT ATTACHMENT Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1998-2017 - IMRI SHORT HD ATTACHMENT Product Usage: Pneumatic system 2 05/04/2017 The Anspach Effort, Inc.
Z-1966-2017 - KEYLESS DRIVER, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
Z-1961-2017 - LARGE CRANIOTOME, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
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