Recall company profile

Orthofix, Inc. Recalls

Overview of recall records associated with Orthofix, Inc., including dates, categories and classifications where available.

22recall records
Jun 13, 2018latest record date
Apr 18, 2018earliest record date

Recall history in this database

Classification mix: Class II: 22.

Medical DeviceApr 18, 2018

Orthofix recall — FDA Z-1363-2018

Orthofix is conducting a voluntary recall of the Connector System Large Set Screw (PN: 79-2002) with affected Lot Numbers 001 and 002, and Small Set Screw (PN: 79-2003) with affected Lot…

Class IIFDA: TerminatedOrthofix, Inc.
Medical DeviceApr 18, 2018

Orthofix recall — FDA Z-1364-2018

Orthofix is conducting a voluntary recall of the Connector System Large Set Screw (PN: 79-2002) with affected Lot Numbers 001 and 002, and Small Set Screw (PN: 79-2003) with affected Lot…

Class IIFDA: TerminatedOrthofix, Inc.

Understanding this recall history

This page summarizes recall records in which the official source identifies Orthofix, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.

Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.