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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 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-1940-2017 - 19cm Attachment, Black Max Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1941-2017 - BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1942-2017 - IMRI AIR CONTROL Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1943-2017 - IMRI MOTOR Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1944-2017 - XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
Z-1945-2017 - XMAX Motor, High Strength Hose Product Usage: Pneumatic 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-1947-2017 - Electric Handpiece EM Hand Control 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-1949-2017 - Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system 2 05/04/2017 FEI # 1045834
The Anspach Effort, Inc.
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