Materialise USA LLC: Medical Device Recall in 2022 - (Recall #: Z-1569-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208

Product Classification:

Class II

Date Initiated: July 13, 2022

Date Posted: August 31, 2022

Recall Number: Z-1569-2022

Event ID: 90704

Reason for Recall:

MU22-INA-DUQ case was labeled as MU22-INA-DUQ but was shipped with the Anatomical Model of case MU22-NOF-SAK

Status: Completed

Product Quantity: 1 unit

Code Information:

Unique Device Identifier (01)05420060352089(10)MU22INADUQ Lot Number: MU22-INQ-DUQ

Distribution Pattern:

US Nationwide distribution in the state of MD.

Voluntary or Mandated:

Voluntary: Firm initiated