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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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23
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 5.9CM 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 12.6CM TAPERED 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 6.1CM 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 B-SAGITTAL ASSEMBLY 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 26.65CM ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 7.5CM ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 8CM ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 13.5CM ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 14CM ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 10.5CM ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 11CM ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 90 DEG RIGHT ANGLE ATTACH, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls CONTRA ANGLE ATTACHMENT, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 9.4CM MICRO REVISION ATTACH, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 16.5CM MICRO REVISION ATTACH, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 22CM MICRO REVISION ATTACH, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls KEYLESS DRIVER, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 16CM MIN INVASIVE ATTACH, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls ADJUSTABLE DRILL GUIDE, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls GREEN ROTATING CRANIOTOME, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls STANDARD CRANIOTOME, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls LARGE CRANIOTOME, BLACK MAX
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 11.25CM ATTACHMENT, BLACK MAX
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
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 7.2cm Adjustable Drill Guide 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 System Console, Single Port, no irrigation
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls System Console, Single Port, with irrigation 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 Console, 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 Foot Control without Switches, SC2100 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 Foot Control, SC2100 Product Usage: Electric system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.