RegWardenFDA facility compliance records
Recall

Class II — Orthofix, Inc

Recalling firmORTHOFIX SRL
Registered facilityORTHOFIX SRL (the firm's only registered facility)
ClassificationClass II
StatusTerminated
ReasonThere is a possibility that the Set Screw (p/n 90-2923) sub-component of the Parallel Rod Connector Assembly (p/n 52-6800) & Axial Rod Connector (p/n 52-6700) may crack during final tightening. Orthofix Inc received six (6) customer complaints related to set screw cracking between November 15, 2010 and December 2012.
ProductFirebird Spinal Fixation System, Parallel Rod Connector (52-6800) and Axial Rod Connector (52-6700). Product Usage: The connector assemblies allow for rod components to be connected side-to-side, or end-to-end and eliminate the need of rebuilding the entire system with a longer rod in order to include the new vertebral levels.
Quantity565 total (287 PN 52-6800 and 278 PN 52- 6700)
DistributionWorldwidewide Distribution - USA Nationwide including Puerto Rico and the countries of: Australia, Lebanon, Germany, Spain, Sweden and Israel.
Initiated2013-02-01
Classified2013-02-28
Terminated2013-07-01
Recall numberZ-0896-2013
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class II recall — Orthofix, Inc (Z-0896-2013).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/64265/

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