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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 103 Results
Related Medical Device Recalls
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Product Description
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Class
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FDA Recall
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Z-1950-2017 - eMax2 Motor Assembly Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1951-2017 - eMax2 Hybrid Hand Control Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1952-2017 - eMax2 PLUS Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1953-2017 - Foot Control, SC2100 Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1954-2017 - Foot Control without Switches, SC2100 Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1955-2017 - Console, eMax2 Plus Product Usage: Electric system 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-1957-2017 - System Console, Single Port, no irrigation 2 05/04/2017 The Anspach Effort, Inc.
Z-1958-2017 - 7.2cm Adjustable Drill Guide Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1959-2017 - 19CM ATTACHMENT, BLACK MAX 2 05/04/2017 The Anspach Effort, Inc.
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