ProPlan CMF Anatomical recall
ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
Why was ProPlan CMF Anatomical recalled?
MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Unique Device Identifier (01)05420060352089(10)MU22INADUQ Lot Number: MU22-INQ-DUQ
- Product
- ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208
- Recalling firm
- Materialise USA LLC
- Quantity
- 1 unit
- Distribution
- US Nationwide distribution in the state of MD.
- Recall date
- August 31, 2022
- Classification
- Class II
- Status
- Completed
- Agency
- FDA (device)