FDA recall Z-0334-2022

Orchestrate Orthodontic Technologies, Inc. · Class II · device

Product

O3D ORCHESTRATE Orthodontic Technologies User Manual and Data Processing Instructions (model preparation for tooth movement) MKT-LB-002 Rev 1 for Orchestrate3d Software v.3.1 - v5.0.4

Reason for recall

Due to product label/labeling being altered from it's approved state.

Distribution

Worldwide distribution - U.S. Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NV, NY, OH, OK, OR, PA, TN, TX, UT, VA, WA, and WI. The countries of Argentina, Australia, Bolivia, Brazil, Canada, Costa Rica, India, Ireland, Mongolia, New Zealand, Pakistan, Spain and Thailand.

Key facts

Status
Terminated
Initiation date
2021-11-11
Report date
2021-12-15
Termination date
2024-01-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Rialto, CA, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0334-2022