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 Nov 20, 2013

Cutting Bur Chart (part number 20-0019) utilized with the Electric and Pneumatic Motor Systems including: MicroMax Motor Systems, XMax Motor Systems, EMax2 Motor Systems, and Emax2Plus Motor Systems, all models and serial numbers. Product Usage: Indication for use is cutting and shaping bone
FDA Devices Moderate Nov 20, 2013

Pneumatic Systems Operating Manual (part numbers 19-0005) utilized with the Pneumatic Motor Systems including: BlackMax Motor Systems, MicroMax Systems and XMax Motor Systems all models and serial numbers. Product Usage: Indication for use is cutting and shaping bone.
FDA Devices Moderate Jul 10, 2013

***REF SC2100***eMax 2 Plus Console***SN G 10307653002*** Product Usage: The RPM of the Motor Handpiece may be less than 80,000 RPM (approximately 72,000 RPM) in the free running state when using the optional Hand Control. The low Motor Handpiece RPM would only be experienced in the Free running state (Hand Control fully depressed and no load on the cutting bur). This condition would not affect the power output of the Handpiece in the loaded working range (typically 50,000 to 70,000 RPM.
FDA Devices Moderate Jul 10, 2013

***REF SC2102***eMax 2 Plus Console, Single Port, no Irrigation***SN G16307882402*** Product Usage: The eMax console is intended to operate the eMax system which is used for cutting and shaping bone including spine and cranium. The RPM of the Motor Handpiece may be less than 80,000 RPM (approximately 72,000 RPM) in the free running state when using the optional Hand Control. The low Motor Handpiece RPM would only be experienced in the Free running state (Hand Control fully depressed and no
FDA Devices Moderate Jul 10, 2013

***REF SC2101***eMax 2 Plus Console, Single Port, with Irrigation***SN G17307901802*** Product Usage: The RPM of the Motor Handpiece may be less than 80,000 RPM (approximately 72,000 RPM) in the free running state when using the optional Hand Control. The low Motor Handpiece RPM would only be experienced in the Free running state (Hand Control fully depressed and no load on the cutting bur). This condition would not affect the power output of the Handpiece in the loaded working range (typi
FDA Devices Moderate Jun 5, 2013

***REF S-3D*** 3mm Diamond Ball. Used for cutting and shaping bone.
FDA Devices Moderate Feb 13, 2013

Anspach Effort, Inc., 98-0061 MA-15C Bearing Sleeve with Removable Bur Guard. A reusable device used with dissection tools; designed for Transphenoidal and Skull base procedures.
FDA Devices Moderate Oct 24, 2012

"***Electric Systems Foot Control****Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
FDA Devices Moderate Oct 24, 2012

"***Electric Systems Foot Control with Direction and Irrigation***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
FDA Devices Moderate Oct 24, 2012

"***Electric Systems Foot Control with Direction Only***Rx Only***" Product Usage: Cutting and shaping bone including bones of the spine and cranium.
FDA Devices Moderate Aug 1, 2012

.***ANSPACH***Sterile. REF SHD-4820DS***QTY: 1, 4.8 mm x 2mm Twist Drill with Depth Stop. Use with SHORT-HD Attachment ***RX Only Product Usage: Cutting and shaping bone including bones of the spine and cranium.

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