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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 8.0cm Medium Attachment 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 Minimal Access Straight Driver 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 Minimal Access 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 Minimal Access Attachment 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 Bearing Sleeve, 19CM Straight Taper 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 Bearing Sleeve, 15CM Straight Taper 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 Bearing Sleeve, 15CM Straight 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 Bearing Sleeve, 15CM Curved 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 Bearing Sleeve, 10CM Straight 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 Bearing Sleeve, 10CM Curved 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 10.5cm Long Attachment 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 12.4cm Heavy Duty Long Heavy Short Attachment 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 10.5cm Long Attachment, Non-Tapered End 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 11.0cm Long Attachment 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 SHORT HD ATTACHMENT 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 SHORT ATTACHMENT 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 CRANI-A ATTACHMENT 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 Keyless Driver 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 Chuck Driver System
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Compact Speed Reducer, 60:1 Black Max
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Compact Speed Reducer, 60:1
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Pediatric Craniotome
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Rotating Large Craniotome
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Large Craniotome 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 Rotating Adult Craniotome 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 6.5CM ADLT CRANI, THIN FT PLATE 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 Adult Craniotome 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 6.8cm Controlled Depth Attachment 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 8.2CM 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 PEDIATRIC CRANIOTOME, BM Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.