PlainRecalls

The Anspach Effort, Inc.

Compiled from official public sources by the publisher.

261 recalls on record · Latest: Jan 18, 2023

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Agency notice ledger

Federal filing book The Anspach Effort, Inc. HEAVY-BOOK · SINGLE-AGENCY

#46 of 14,151 · 261 notices · 0.250% archive

  • BOOK 261 notices
  • RANK #46 of 14,151
  • SHARE 0.250% archive
  • AGENCY FDA Devices (261)
  • CAT medical devices
  • CATS 1 category
  • LATEST Jan 18, 2023
  • PHOTO Hyundai

Nearest notice-volume peer: Hyundai (0 notice gap)

The Anspach Effort, Inc. accounts for about 0.250% of the 104,423-notice archive on 261 distinct filings — a heavy share signal beside absolute volume. FDA · CPSC · USDA FSIS · NHTSA notice stamps for this firm. Read with this firm → · Dominant category → · Similar-volume firm →

Where The Anspach Effort, Inc. sits among 14,151 recalling firms

The Anspach Effort, Inc. ranks 46th of 14,151 tracked firms by distinct recall-event count. Archive size reflects filing volume, not inherent product danger.

The Anspach Effort, Inc. vs all firms by recall-notice count

Where this firm's archive sits among every tracked recalling manufacturer

261 46th of 14151 higher than 14,105 of 14,151 firms

Firms, banded by distinct federal recall-event inventory

Each bar is a band; taller bars hold more firms. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source FDA · CPSC · USDA FSIS · NHTSA federal recall filings · 2026-09-13

The Anspach Effort, Inc. in the notice-volume neighbourhood

Distinct federal recall events among this firm and nearest nationwide peers

notices

What this shows The Anspach Effort, Inc. holds about 0.250% of archive notices alongside 261 distinct filings.

Source FDA · CPSC · USDA FSIS · NHTSA filings aggregated by PlainRecalls As of September 2026
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 including the spine and cranium
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 including the spine and cranium
FDA Devices Moderate Jan 18, 2023

7.5 cm Large Craniotome Attachment Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-L Intended for cutting and shaping bone including the spine and cranium
FDA Devices Moderate Jan 18, 2023

6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-R intended for cutting and shaping bone including the spine and cranium
FDA Devices Moderate Jan 18, 2023

6.5 cm Adult Craniotome, Thin Foot Plate Attachment. Use with XMax¿, microMax, and eMax¿ Systems Ref: CRANI-A-01 intended for cutting and shaping bone including the spine and cranium by trained medical/surgical personnel
FDA Devices Moderate Jan 18, 2023

6.5 cm Adult Rotating Craniotome Attachment. Use with XMax¿, microMax, and eMax¿ Systems. Ref: CRANI-A Intended for cutting and shaping bone including the spine and cranium
FDA Devices Moderate Jan 18, 2023

Adult Craniotome Ref: CRANI-A-G1 Intended for cutting and shaping bone including the spine and cranium
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 tissue or bone and soft tissue.
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

The Anspach Effort, Inc. carries an outsized archive share

Drug and device firms outside this manufacturer and state, matched by notice volume and category footprint.

Similar recall count

Nearest multi-notice firms by distinct-event totals (261 here — heavy-book).

Hyundai 261 Cook Inc. 264 Smith & Nephew, Inc. 258 Honda 265 Hospira Inc. 257

Similar medical devices volume

Nearest multi-notice firms in the same narrow category lane.

Cook Inc. 264 Smith & Nephew, Inc. 258 Intuitive Surgical, Inc. 257 Biomet, Inc. 255

Frequently Asked Questions

How many federal recall notices name The Anspach Effort, Inc.? ▼
PlainRecalls indexes 261 distinct federal recall events naming The Anspach Effort, Inc., aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (archive as of September 2026). That count is an issuance inventory, not a hazard score.
Where does The Anspach Effort, Inc. sit among other recalling firms? ▼
The Anspach Effort, Inc. ranks #46 of 14,151 by distinct recall-event count among 14,151 firms in this archive (99th percentile of firms with fewer notices). Rank tracks filing frequency, not product danger.
Which agency issues most of The Anspach Effort, Inc.'s notices? ▼
FDA Devices accounts for 261 of this firm's 261 indexed notices.
What product category dominates The Anspach Effort, Inc.'s filing book? ▼
Filings for The Anspach Effort, Inc. span 1 product category, led by medical devices. Browse that category archive for peer firms and related notices.
Is a higher notice count more dangerous? ▼
No. Archive size reflects how often federal agencies publish recalls naming the firm — reporting volume, coverage, and product range all move the number. Always verify the individual notice with the issuing agency before acting on a specific product.
The Anspach Effort, Inc.: 261 federal recall notices aggregated from FDA, CPSC, USDA FSIS, and NHTSA filings (lead agency FDA Devices). Verify individual notices with FDA directly before acting on a specific recall.

Firm-level totals aggregate distinct federal recall events naming The Anspach Effort, Inc.; individual notices remain authoritative on each linked recall page.

Methodology · Corrections · FDA · CPSC · USDA FSIS · NHTSA · Archive as of September 2026