Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Product Catalog (part number 20-0020) utilized with the Electric and Recalled by The Anspach Effort, Inc. Due to Anspach Effort, Inc. Palm Beach Gardens, FL initiated...
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
Product Catalog (part number 20-0020) 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.
Quantity: 2,020
Why Was This Recalled?
Anspach Effort, Inc. Palm Beach Gardens, FL initiated a correction of its medical Device labeling for its Pneumatic Systems Operating Manual, Cutting Burr Chart and Product Catalog due to a recent review of their regulations and compliance requirements that determined the claim that the device is capable of dissection of biometals, bioplastics and cement has been verified, but is is not part of th
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About The Anspach Effort, Inc.
The Anspach Effort, Inc. has 261 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report