PlainRecalls

The Anspach Effort, Inc.

182 recalls on record · Latest: Jan 18, 2023

The Anspach Effort, Inc. Recall Insight

The Anspach Effort, Inc. appears on 182 federal recall records indexed by PlainRecalls, out of 83,949 total recalls tracked across the FDA, CPSC, NHTSA, and USDA FSIS. That represents approximately 0.217% of the federal archive — a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Jan 18, 2023, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 48 of 50 entries — unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from May 10, 2017 to Jan 18, 2023.

Manufacturer-level browsing is useful when monitoring a single firm for patterns — whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current — deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement — always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Jan 18, 2023

Pediatric Craniotome Ref:CRANI-P-G1

FDA Devices Moderate Jan 18, 2023

Adult Craniotome, Large Ref: CRANI-L-G1 Intended for cutting and shaping bone including the spine and cranium

FDA Devices Moderate Jan 18, 2023

7.5 cm Large Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-L-R Intended for cutting and shaping bone i…

FDA Devices Moderate Jan 18, 2023

6.5 cm Pediatric Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-P Intended for cutting and shaping bone includin…

FDA Devices Moderate Jan 31, 2018

OSCILLATING SAW ATTACHMENT Surgical instrument motors and accessories/attachments are intended for use during surgical procedures to cut hard tiss…

FDA Devices Moderate May 10, 2017

Keyless Driver Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

14cm QD Angle Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Electric Handpiece EM Hand Control Product Usage: Electric system

FDA Devices Moderate May 10, 2017

6.8cm Controlled Depth Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

SMALL ATTACHMENT, J-LATCH

FDA Devices Moderate May 10, 2017

IMRI AIR CONTROL Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

14cm QD Angle Attachment Product Usage: Product attachment

FDA Devices Moderate May 10, 2017

XMAX Motor, High Strength Hose Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

12.6CM TAPERED ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Rotating Adult Craniotome Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Foot Control without Switches, SC2100 Product Usage: Electric system

FDA Devices Moderate May 10, 2017

STANDARD CRANIOTOME, BLACK MAX

FDA Devices Moderate May 10, 2017

11cm QD Angle Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

System Console, Single Port, with irrigation Product Usage: Electric system

FDA Devices Moderate May 10, 2017

Rotating Large Craniotome

FDA Devices Moderate May 10, 2017

BLACKMAX-NEURO LOW PRESSURE Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 15CM Straight Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

IMRI SHORT ATTACHMENT Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

90 degree Contra Angle Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Foot control irrigation system Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

19cm Attachment, Black Max Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Autolube-III with Foot Guard Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

11.0cm Long Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Autolube-III with Irrigation Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

5.0cm Short Attachment

FDA Devices Moderate May 10, 2017

Large Craniotome Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

8cm QD Angle Attachment

FDA Devices Moderate May 10, 2017

13.5CM ANGLE ATTACHMENT, BLACK MAX

FDA Devices Moderate May 10, 2017

26.65CM ATTACHMENT, BLACK MAX

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 10CM Straight Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

Autolube-III with 20ft hose Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

eMax2 PLUS Product Usage: Electric system

FDA Devices Moderate May 10, 2017

Reciprocating MICRO SAW

FDA Devices Moderate May 10, 2017

Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system

FDA Devices Moderate May 10, 2017

Compact Speed Reducer, 60:1

FDA Devices Moderate May 10, 2017

6.1CM ATTACHMENT, BLACK MAX Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

7.5cm QD Angle Attachment

FDA Devices Moderate May 10, 2017

10.5cm Long Attachment, Non-Tapered End Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

10.5cm Long Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

9.4CM MICRO REVISION ATTACH, BLACK MAX

FDA Devices Moderate May 10, 2017

CONTRA ANGLE ATTACHMENT, BLACK MAX

FDA Devices Moderate May 10, 2017

ADJUSTABLE DRILL GUIDE, BLACK MAX

FDA Devices Moderate May 10, 2017

Bearing Sleeve, 19CM Straight Taper Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

8.0CM Heavy Duty Medium Attachment Product Usage: Pneumatic system

FDA Devices Moderate May 10, 2017

GREEN ROTATING CRANIOTOME, BLACK MAX

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Data Sources

  • Source: FDA + CPSC + NHTSA + USDA FSIS — federal recall filings naming this firm. Verify with FDA, CPSC, NHTSA, or USDA FSIS directly.
  • Source: PlainRecalls Manufacturer Index — firm-level aggregation across all four federal recall feeds