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The Anspach Effort Recalls
261 recalls on record · August 1, 2012 to January 18, 2023 · Medical Devices
Recalls by year
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Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls eMax2 PLUS Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls eMax2 Hybrid Hand Control Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls eMax2 Motor Assembly Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Electronic Foot Control with Direction Switch Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Electric Handpiece EM Hand Control Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls XMAX Motor, High Strength Hose Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls IMRI MOTOR Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls IMRI AIR CONTROL Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 19cm Attachment, Black Max Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Autolube-III with NK Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Autolube-III with Irrigation Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Autolube-III with Foot Guard Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls AL-III-DISS Adapter Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Autolube-III with 20ft hose Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Autolube-III Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Foot control irrigation system Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls AL-III W/ male disconnect and 20ft hose Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 14cm QD Angle Attachment Product Usage: Product attachment
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
October 5, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive
Hazard: There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to generate excessive internal pressure that may cause the products to burst.
October 5, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls Light Adaptor for Small Battery Drive and Small Battery Drive II.
Hazard: There was a potential for the Adaptor and Light Adaptor for Small Battery Drive and Small Battery Drive II to generate excessive internal pressure that may cause the products to burst.
September 28, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls G1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.
Hazard: The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
September 28, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls G1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including spine and cranium.
Hazard: The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
September 28, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls G1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M; For cutting and shaping bone including spine and cranium.
Hazard: The firm discovered on March 4, 2016 that several product codes were inadvertently left off of Hold 1503.
September 28, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls G1 Dissection Tool - 7mm FBALL L; For cutting and shaping bone including spine and cranium.
Hazard: Product Code L- 7B-G1 was inadvertently released off of hold status and the affected products were distributed.
July 27, 2016Medical DevicesFDA
The Anspach Effort, Inc. recalls Anspach G1 High Speed Electric Handpiece Air Cooled (eG1A) Use for cutting and shaping bone including bones of the cr
Hazard: The graphics at the attachment interface indicating locked and unlocked position are reversed.