Events

Recall of Device Recall Hip Prostheses

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Ortho Development Corporation.

What is this?

A correction or removal action taken by a manufacturer to address a problem with a medical device. Recalls occur when a medical device is defective, when it could be a risk to health, or when it is both defective and a risk to health.

Learn more about the data here
  • Type of Event
    Recall
  • Event ID
    25395
  • Event Risk Class
    Class 2
  • Event Number
    Z-0567-03
  • Event Initiated Date
    2002-12-26
  • Event Date Posted
    2003-02-25
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2003-04-22
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=25739
  • Notes / Alerts
    U.S. data is current through June 2018. All of the data comes from the U.S. Food and Drug Administration, except for the category Manufacturer Parent Company.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel data.
  • Extra notes in the data
  • Reason
    Cleaning agent residue from packaging material was adhering to implantable hip stems.
  • Action
    Consignees were notified on 12/26/2002 via telephone and e-mail.

Device

Device Recall Hip Prostheses
  • Model / Serial
    Catalog # 111-0917, Lot # OD-22372. Catalog # 111-1015, Lot # OD-21589, OD-21589-1 Catalog # 111-1017, Lot # OD-23209. Catalog # 111-1019, Lot # OD-23235. Catalog # 111-1115, Lot # OD-22050. Catalog # 111-1117, Lot # OD-23205, OD-23205-1, OD-23298. Catalog # 111-1119, Lot # OD-22846, W002952, OD-23222. Catalog # 111-1217, Lot # OD-23207, OD-23208, OD-23299. Catalog # 111-1219, Lot # OD-22847, OD-20859-1, OD-23230, OD-22847-1. Catalog # 111-1221, Lot # OD-23254, OD-23249, Catalog # 111-1223, Lot # OD-18165, W002524. Catalog # 111-1319, Lot # OD-23231, OD-23231-1.  Catalog # 111-1321, Lot # OD-23247. Catalog # 111-1421, Lot # OD-23250, OD-23255. Catalog # 111-1423, Lot # OD-23256. Catalog # 111-1425, Lot # OD-20837-1, W002683. Catalog # 111-1625, Lot # OD-21873, OD-19626-1, OD-22537.
  • Product Classification
    Orthopedic Devices
  • Distribution
    TX and Japan
  • Product Description
    Hip Prosthesis as a component of Primaloc Cementless/Collarless Hip System
  • Manufacturer
    Ortho Development Corporation

Manufacturer

Ortho Development Corporation
  • Manufacturer Address
    Ortho Development Corporation, 12187 Business Park Drive, Draper UT 84020
  • Source
    USFDA