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Nuvasive Specialized Orthopedics Inc recalls NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur Trochanter 10 Degree Bend Component of
Recalled October 14, 2020 · FDA recall Z-0069-2021 · Nuvasive Specialized Orthopedics
Hazard
During explantation, standard removal tools can generate sufficient forces to cause distal plug to disassociate from the bone transport system. · FDA Class II
Units
41 total units
Sold at
Worldwide distribution. US nationwide, Austria, Australia, Canada, Switzerland, Denmark, Spain, France, United Kingdom, Germany, UAE, Luxembourg, Israel, Netherlands.
Description
During explantation, standard removal tools can generate sufficient forces to cause distal plug to disassociate from the bone transport system.
Product
NUVASIVE SPECIALIZED ORTHOPEDICS, INC. Precice Bone Transport Antegrade Femur Trochanter 10 Degree Bend Component of the orthopedic Precice Bone Transport System of intramedullary nail, locking screws, reusable instruments, and hand-held External Remote Controller (ERC).
Manufacturer(s)
Nuvasive Specialized Orthopedics Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →