Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ProPlan CMF Anatomical Model Recalled by Materialise USA LLC Due to MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was...
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 Materialise USA LLC directly.
Affected Products
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Quantity: 1 unit
Why Was This Recalled?
MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Materialise USA LLC
Materialise USA LLC has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report