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U.S. Department of Health and Human Services

Medical Device Recalls
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101 to 103 of 103 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-1951-2017 - eMax2 Hybrid Hand Control Product Usage: Electric system 2 05/04/2017 The Anspach Effort, Inc.
Z-1950-2017 - eMax2 Motor Assembly 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.
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