Class II — Potential Health Hazard

Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

ANSPACH - Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1 Dissection Tools are not compatible with all...

Date: April 13, 2015
Company: The Anspach Effort, Inc.
Status: Terminated
Source: FDA (Device)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact The Anspach Effort, Inc. directly.

Affected Products

ANSPACH - Fluted Ball; 9MM REF L-9B-G1 Cutting shaping bone including spine and cranium.

Quantity: 353 tools.

Why Was This Recalled?

G1 Dissection Tools are not compatible with all attachments listed on the labeling; G1 cutting tools are labeled with a Specified Shaft Exposure which may not be consistent when used with each attachment on the product label. Shaft exposure may be greater.

Where Was This Sold?

This product was distributed to 17 states: AZ, CA, CO, FL, GA, IL, KY, LA, MN, MO, NJ, NY, NC, OH, OR, PA, TX

Affected (17 states)Not affected

About The Anspach Effort, Inc.

The Anspach Effort, Inc. has 261 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report