Materialise recalls ProPlan CMF Anatomical Models with incorrect case labels that could lead to confusion in identification. Affected units have a specific identification number and lot number.
MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK
Materialise is recalling ProPlan CMF Anatomical Models with incorrect case labels. This could cause confusion in identifying the correct product, but it does not pose a safety risk.
The case label on the product was incorrectly labeled as MU22-INA-DUQ but was shipped with the Anatomical Model case MU22-NOF-SAK. This mismatch could lead to confusion about which product is being used, but it does not cause physical harm.
Users of the ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear with identification number SD900.208 are affected. Those who rely on precise product identification for medical or educational purposes may be most at risk.
Check for the identification number SD900.208 and lot number MU22-INQ-DUQ on the product. The case label should read MU22-INA-DUQ but was shipped with MU22-NOF-SAK.
Look for the identification number SD900.208 and lot number MU22-INQ-DUQ on the product.
No, this recall is for labeling confusion only and does not pose a safety risk.
Check the product label for the identification number SD900.208 and lot number MU22-INQ-DUQ. If the case label shows MU22-NOF-SAK instead of MU22-INA-DUQ, it is affected.
The product has the identification number SD900.208 and lot number MU22-INQ-DUQ with a case label mismatch between MU22-INA-DUQ and MU22-NOF-SAK.
We’ve drafted a message you can send Materialise to request your refund or repair — edit it as you like.
Subject: Recall Z-1569-2022 — Materialise Materialise Hello, I own a Materialise that is covered by recall Z-1569-2022 from Materialise. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
