Orthofix, Inc: 8 recalls on record

Recalls filed with 1 agency: FDA (8).

First recall on record: March 6, 2013. Most recent: June 13, 2018.

Risk classification: Class II: 8

Most recent recalls

DateAgencyProduct
June 13, 2018FDAL-Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Left or Right (Part Number): a…Z-2130-2018
June 13, 2018FDARival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOF…Z-2116-2018
June 13, 2018FDAY-Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Size (Part Number): a) Small (…Z-2135-2018
September 20, 2017FDAFirebird NXG Spinal Fixation System Decorticating Planer, Catalog #36-1334, non-sterile, …Z-3127-2017
March 5, 2014FDAAzure Anterior Cervical Plate System, 2-Level Plate, 36 mm, Implant Grade Titanium and Ni…Z-1089-2014
February 5, 2014FDAOrthofix Firebird Spinal Fixation System Instrumentation Modular Screw Driver, Prod…Z-0855-2014
March 6, 2013FDAOrthofix ISKD Limb Lengthener. ISKD - Intramedullary Skeletal Kinetic Distractor. T…Z-0895-2013
March 6, 2013FDAFirebird Spinal Fixation System, Parallel Rod Connector (52-6800) and Axial Rod Connector…Z-0896-2013

Questions about this company

How many recalls does Orthofix, Inc have?
Recalert has 8 U.S. recalls on record for Orthofix, Inc, published between March 6, 2013 and June 13, 2018.
What was the most recent Orthofix, Inc recall?
FDA recall Z-2130-2018, published June 13, 2018: L-Plate, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Left or Right (Part Number): a) Left (003-E-00001L); b) Right (003-E-00001R)
Which agencies have handled Orthofix, Inc recalls?
Orthofix, Inc appears as the recalling firm in recalls from: FDA (8).

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