Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Anspach MIA 16 (16cm Minimally Invasive Attachment) Recalled by The Anspach Effort, Inc. Due to Product did not reach expected sterility assurance level
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 MIA 16 (16cm Minimally Invasive Attachment), Rx Only MIA16 attachments are intended for use with Motor Systems for cutting and shaping bones, including the spine and cranium.
Quantity: 183
Why Was This Recalled?
Product did not reach expected sterility assurance level
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