Data Foundry

Medical device recalls 2018

Rival Reduce Kit Locking and Non-Locking Screw D 2 — Class II medical device recall Z-2116-2018

Terminated recall by Orthofix, Inc, reported 2018-06-13, distributed in CA, DC, FL, GA, IL, IN, LA, MD…. Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating Syste

Recall numberZ-2116-2018
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmOrthofix, Inc, Lewisville, TX, United States
Recall initiated2018-04-06
Classified2018-06-07
Reported by FDA2018-06-13
Terminated2021-06-30
DistributedCA, DC, FL, GA, IL, IN, LA, MD, MI, MN, NC, NJ, NV, OH, OK, PA, SC, TX, VA
Quantity50
Reason classesdevice malfunction
UPC / GTIN / UDI-DI18056099648592
Model numbers000-K-011C

Product

Rival Reduce Kit Locking and Non-Locking Screw D 2.0MM, D 2.7MM, Sterile, Rx Only, ORTHOFIX S.r.r. Italy on label, Part Number: 000-K-011C

Reason for recall

Firm is conducting a voluntary recall of the Rival Reduce Fracture Plating System and Rival View Plating System. As the result of a complaint investigation, the locking screws were confirmed to not properly engage the plates during surgery.

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2116-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.