Events

Recall of Device Recall Stryker Orthopaedics Restoration Gap Plate Screw

According to U.S. Food and Drug Administration, this recall involved a device in United States that was produced by Stryker Howmedica Osteonics Corp..

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
    52713
  • Event Risk Class
    Class 3
  • Event Number
    Z-2135-2009
  • Event Initiated Date
    2009-06-26
  • Event Date Posted
    2009-09-14
  • Event Status
    Terminated
  • Event Country
    United States
  • Event Terminated Date
    2010-07-27
  • Event Source
    USFDA
  • Event Source URL
    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfres/res.cfm?id=83760
  • 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 was added by ICIJ.
    The parent company information is based on 2017 public records.
  • Extra notes in the data
    Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate - Product Code MEH
  • Reason
    Raw material supplied by a third party used to manufacture various medical devices does not comply with metallurgical requirements outlines in astm standard for titanium surgical implants.
  • Action
    Stryker Orthopaedics issued "Urgent Product Recall" letters via Federal Express priority overnight beginning June 26, 2009 to Branches, Hospital Risk Management and Chief of Orthopaedics and Surgeons. All users are requested to examine their inventory, retrieve all affected product and return for reconciliation to Stryker Orthopaedics. Users are also requested to complete the enclosed Product Accountability Form and fax with necessary information to the firm at 1-201-831-6069. For further information, contact Stryker Orthopaedics at 1-201-831-5970.

Device

Device Recall Stryker Orthopaedics Restoration Gap Plate Screw
  • Model / Serial
    Catalog number: 2080-0020; GAP PLATE SCREWS T0WMKE 01-Jul-2013 GAP PLATE SCREWS T0XMKE 02-Jul-2013 GAP PLATE SCREWS T10MKE 02-Jul-2013 GAP PLATE SCREWS T0YMKE 02-Jul-2013 GAP PLATE SCREWS 22RMLE 07-Jul-2013 GAP PLATE SCREWS 229MLE 07-Jul-2013 GAP PLATE SCREWS 22PMLE 08-Jul-2013 GAP PLATE SCREWS D01MLE 21-Jul-2013 GAP PLATE SCREWS AYYMLE 23-Jul-2013 GAP PLATE SCREWS PLAMME 27-Aug-2013 GAP PLATE SCREWS PN2MME 27-Aug-2013 GAP PLATE SCREWS PL8MME 28-Aug-2013 GAP PLATE SCREWS PL9MME 28-Aug-2013 GAP PLATE SCREWS PN1MME 28-Aug-2013 GAP PLATE SCREWS 7DXMNE 16-Sep-2013 GAP PLATE SCREWS MET9H4 18-Dec-2013 GAP PLATE SCREWS MET9X8 18-Dec-2013 GAP PLATE SCREWS MET9X7 22-Dec-2013 GAP PLATE SCREWS METL9Y 28-Dec-2013 GAP PLATE SCREWS METLA0 30-Dec-2013 GAP PLATE SCREWS MET9H5 30-Dec-2013 GAP PLATE SCREWS MET9X9 30-Dec-2013 GAP PLATE SCREWS MET9XA 30-Dec-2013 GAP PLATE SCREWS MHA4YT 14-Jan-2014 GAP PLATE SCREWS MHA4YR 18-Jan-2014 GAP PLATE SCREWS MHA55K 18-Jan-2014 GAP PLATE SCREWS MHA55L 18-Jan-2014 GAP PLATE SCREWS MHA55H 18-Jan-2014
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Worldwide Distribution
  • Product Description
    Stryker Orthopaedics Restoration Gap Plate Screw; || Dia. 6.5 mm, Lnth 20 mm; || Made in USA, Sterile; || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430
  • Manufacturer
    Stryker Howmedica Osteonics Corp.

Manufacturer

Stryker Howmedica Osteonics Corp.
  • Manufacturer Address
    Stryker Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah NJ 07430
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    USFDA