PlainRecalls

The Anspach Effort, Inc.

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 Aug 5, 2015

ANSPACH - 5MM Fluted Ball, 2 mm Shaft Exposure; REF M-5B-2-G1. Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH -1.5MM x 7.5MM Cylindrical Carbide Drum, Extends 25MM; REF S-15DRMC-L-G1. Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - Fluted Barrel; 8MM x 12.5MM REF L-8BA-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 7MM Extra Coarse Diamond Ball; REF M-7DX-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 6MM x 11.3MM Fluted Barrel; REF M-6BA-A-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 3MM Course Diamond Ball, 2 MM Shaft Exposure; REF M-3DC-2-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 6MM Coarse Diamond Ball, 2 mm Shaft Exposure; REF M-6DC-2-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH -3MM Coarse Diamond Ball,72MM Shaft Exposure; REF S-3SDC-22-G1. Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 3MM Fluted Ball, 2 MM Shaft Exposure; REF M-3SB-2-G1. Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 5MM x 11.3MM Fluted Barrel; REF M-5BA-A-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - 5MM Fluted Ball, 2MM Shaft Exposure; REF S-5B-2-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate Aug 5, 2015

ANSPACH - Fluted Drum, Side Cut only 10MM x 14MM , REF L-10DRC-G1 Cutting shaping bone including spine and cranium.

FDA Devices Moderate May 6, 2015

Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number: 532.021 for orthopedic surgery.

FDA Devices Moderate Feb 11, 2015

16cm Minimally Invasive Attachment. For use with Motor Systems for cutting and shaping bones, including the spine and cranium. Model MIA16-G1

FDA Devices Moderate Jul 9, 2014

Anspach Pneumatic and Electric Motor Systems. Intended for cutting and shaping bone, including the spine and cranium.

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0033***Custom Autolube Food Guard***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***MA Attachment, Straight version Custom***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0016***eMax 2 Modified Hand Control***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***Custom QD11 Attachment with thinner nose tube***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0023***Custom 5 cm Extension Bearing Sleeve***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***Modified QD11 Attachment with Soft Tissue Protector***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4604-00***3mm Fluted Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-3012-00***13 mm Drill with Depth Stop for Short Heavy Duty Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0022***8 mm Coarse Headless Screw with Driver***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0042***XMax Motor with Custom Hose***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-5000-00***Threaders, Arthroscopic Suture Anchor***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0035***Custom eMax 2 Plus Motor with microMax Disconnect Sleeve***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4601-00***1mm Coarse Diamond Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4605-00***Arthroscopic Suture Anchor assembly with Suture Threader***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0020***Modified Arthroscopic Knotless Suture Anchor Deployment Tool with Suture Puller***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***Arthroscopic Knotless Suture Anchor***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0048***Custom Circular ePLUS-FP***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0019***Modified MDA Tube with MA-D20 Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0034***Custom XMax Motor, Pneumatic with Hand Control and Custom Autolube III IRR Foot Pedal***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-3014-00***4mm Fluted Ball for MRI***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***eMax2 Lower Profile Foot Pedal***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-3101-00***Adjustable 25 Cm Mia Attachment, Custom***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***Custom MCA5-1SD with Extended Exposure***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0037***Custom Device SC2102 with fast stop firmware***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0010***2.37mm Spiral Drill, for Short Attachment (Non-Sterile)***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4603-00***3mm Coarse Diamond Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-4602-00***2mm Coarse Diamond Ball for Adjustable 25cm Mia Attachment***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0001***eMax Hand Control***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF SP-3100-00***5mm Coarse Diamond Ball, 11.5 OAL***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF-98-0056***Custom Device Autolube III modified with a swivel***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0012***Shoulder Implant 011mm Rod, 20cm Long, Custom***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0031***Custom Medium Attachment, with 5 mm Extended Tapered Tip***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0024***Nose Cone Cover***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***1.85mm x 16 mm Fluted Router for MRI***Rx Only*** This device is intended to be used with Anspach Systems

FDA Devices Moderate Jul 2, 2014

ANSPACH***REF 98-0044***Custom Device Speed Reducer with Bumper***Rx Only*** This device is intended to be used with Anspach Systems

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).

Similar medical devices volume

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

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