Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
***REF XMAX***XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort Recalled by The Anspach Effort, Inc. Due to The firm Anspach Effort of Palm Beach Gardens,...
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
***REF XMAX***XMax Handpiece***Rx Only***Manufacturer: The Anspach Effort, Inc. Intended for cutting and shaping bone.
Quantity: 976
Why Was This Recalled?
The firm Anspach Effort of Palm Beach Gardens, FL initiated a voluntary removal of the Pneumatic Drill System, including the motor hand-piece, Auto Lube foot control, without a pressure relief valve (PRV) due to the hand piece's outer hose can rupture without warning if the air flow is blocked during use..
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