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The Anspach Effort Recalls
261 recalls on record · August 1, 2012 to January 18, 2023 · Medical Devices
Recalls by year
12
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14
15
16
17
18
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.
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls Pediatric Craniotome Ref:CRANI-P-G1
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-P Intended for cutt
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-L-R Intended f
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cutting and shaping bone including the spine and cranium
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls 7.5 cm Large Craniotome Attachment Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-L Intended for cutting
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-R intended f
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls 6.5 cm Adult Craniotome, Thin Foot Plate Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-01
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 18, 2023Medical DevicesFDA
The Anspach Effort, Inc. recalls 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-A Intended fo
Hazard: Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment) came out of the attachment, possibly during removal of the attachment, intra-operatively. Failure to follow the recommended inspection intervals provided in the IFU may result in serious patient injury
January 31, 2018Medical DevicesFDA
The Anspach Effort, Inc. recalls OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgica
Hazard: This voluntary recall was initiated because a veterinary unit was physically shipped in error to a non-veterinary customer account.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 20.2cm Heavy Duty Long Heavy Short Attachment
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Sagittal MICRO-SAW
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 5.0cm Heavy Duty Short Attachment
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 5.0cm Short Attachment
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls SMALL ATTACHMENT, J-LATCH
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls SMALL ATTACHMENT, JACOBS CHUCK
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls Reciprocating MICRO SAW
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 7.5cm QD Angle Attachment
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.
May 10, 2017Medical DevicesFDA
The Anspach Effort, Inc. recalls 8cm QD Angle Attachment
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
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: 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 QD Angle 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 11cm QD Angle 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 Oscillating MICRO-SAW 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 90 degree Contra Angle 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 45 degree Contra Angle 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 Otologic Curved Micro 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 Sagittal Saw 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 16cm Minimally Invasive 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 8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system
Hazard: Supplied Directions for Use (DFU) did not contain a recommended service interval.