The Anspach Effort, Inc. recalls

164 recalls on record · latest: December 7, 2022

Official U.S. recall history for The Anspach Effort, Inc., compiled from official government records.

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The Anspach Effort, Inc. recalls Pediatric Craniotome Ref:CRANI-P-G1

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cutting and shaping bone including the spine and cranium

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls 7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-L-R Intended for cu…

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls 6.5 cm Pediatric Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-P Intended for cutting a…

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls 7.5 cm Large Craniotome Attachment Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-L Intended for cutting and s…

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-R intended for cu…

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

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 intend…

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls 6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-A Intended for cut…

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium

December 7, 2022 · Medical device recalls Moderate risk Ball bearings in the CRANI-A (ANSPACH Power Tools Adult Craniotome Attachment)…

The Anspach Effort, Inc. recalls OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical…

September 29, 2017 · Medical device recalls Moderate risk This voluntary recall was initiated because a veterinary unit was physically sh…

The Anspach Effort, Inc. recalls Keyless Driver Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 14cm QD Angle Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Electric Handpiece EM Hand Control Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 6.8cm Controlled Depth Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls SMALL ATTACHMENT, J-LATCH

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls IMRI AIR CONTROL Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 14cm QD Angle Attachment Product Usage: Product attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls XMAX Motor, High Strength Hose Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 12.6CM TAPERED ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Rotating Adult Craniotome Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Foot Control without Switches, SC2100 Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls STANDARD CRANIOTOME, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 11cm QD Angle Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls System Console, Single Port, with irrigation Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Rotating Large Craniotome

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Bearing Sleeve, 15CM Straight Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls IMRI SHORT ATTACHMENT Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 90 degree Contra Angle Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Foot control irrigation system Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 19cm Attachment, Black Max Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Autolube-III with Foot Guard Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 11.0cm Long Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Autolube-III with Irrigation Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 5.0cm Short Attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Large Craniotome Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 8cm QD Angle Attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 13.5CM ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 26.65CM ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Bearing Sleeve, 10CM Straight Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Autolube-III with 20ft hose Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls eMax2 PLUS Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Reciprocating MICRO SAW

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Compact Speed Reducer, 60:1

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 7.5cm QD Angle Attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 10.5cm Long Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 9.4CM MICRO REVISION ATTACH, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls CONTRA ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls ADJUSTABLE DRILL GUIDE, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls GREEN ROTATING CRANIOTOME, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 7.5CM ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 14CM ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls System Console, Single Port, no irrigation

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 12.4cm Heavy Duty Long Heavy Short Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 45 degree Contra Angle Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 90 DEG RIGHT ANGLE ATTACH, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Bearing Sleeve, 15CM Curved Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls IMRI CRANI-A ATTACHMENT Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls eMax2 Motor Assembly Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 16CM MIN INVASIVE ATTACH, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls AL-III-DISS Adapter Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 11CM ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls eMax2 Hybrid Hand Control Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Compact Speed Reducer, 60:1 Black Max

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Electronic Foot Control with Direction Switch Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 10.5cm QD Angle Attachment Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls IMRI MOTOR Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Foot Control, SC2100 Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 22CM MICRO REVISION ATTACH, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Autolube-III with NK Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Adult Craniotome Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 20.2cm Heavy Duty Long Heavy Short Attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 5.0cm Heavy Duty Short Attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Sagittal MICRO-SAW

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Pediatric Craniotome

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 14cm QD Angle Attachment

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Oscillating MICRO-SAW Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 8.2CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 16.5CM MICRO REVISION ATTACH, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls LARGE CRANIOTOME, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls KEYLESS DRIVER, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 10.5CM ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 11.25CM ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 8CM ANGLE ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 7.2cm Adjustable Drill Guide Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls B-SAGITTAL ASSEMBLY Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Minimal Access Straight Driver Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls SMALL ATTACHMENT, JACOBS CHUCK

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Chuck Driver System

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Console, eMax2 Plus Product Usage: Electric system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls 19CM ATTACHMENT, BLACK MAX

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…

The Anspach Effort, Inc. recalls Sagittal Saw Product Usage: Pneumatic system

October 6, 2016 · Medical device recalls Moderate risk Supplied Directions for Use (DFU) did not contain a recommended service interva…