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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 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-1963-2017 - GREEN ROTATING CRANIOTOME, BLACK MAX 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1933-2017 - Foot control irrigation system Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1953-2017 - Foot Control, SC2100 Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1954-2017 - Foot Control without Switches, SC2100 Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1949-2017 - Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1946-2017 - Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1948-2017 - Electronic Foot Control with Direction Switch Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1947-2017 - Electric Handpiece EM Hand Control Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1955-2017 - Console, eMax2 Plus Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1993-2017 - Compact Speed Reducer, 60:1 Black Max 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
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