Onkos Surgical Inc. My3D Personalized Pelvic Implant, Porous, Left REF PV-ACREC-04M
Official notice from a government agency or its published feed.
Reason: Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
Class IIA mid-level FDA recall: the product may cause temporary or reversible health problems. · Ongoing · US Nationwide distribution in the states of North Carolina, and California.
Hazard: Personalized pelvic implants inadvertently mixed up and distributed to incorrect customers.
View the FDA enforcement report ↗ ← All reports