Events

Recall of Device Recall Stryker Orthopaedics Bone 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-2123-2009
  • 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=83748
  • 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
    Screw, fixation, bone - Product Code HWC
  • 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 Bone Screw
  • Model / Serial
    Catalog number: 2030-6550-1; 6.5 CANCELLOUS BONE SCREW 50mm KKMMKE 22-Jun-2013 6.5 CANCELLOUS BONE SCREW 50mm NMXMKE 25-Jun-2013 6.5 CANCELLOUS BONE SCREW 50mm R89MKE 27-Jun-2013 6.5 CANCELLOUS BONE SCREW 50mm 8K6MLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm 8K4MLE 14-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm MAJMLE 25-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm MAHMLE 28-Jul-2013 6.5 CANCELLOUS BONE SCREW 50mm HVWMME 22-Aug-2013 6.5 CANCELLOUS BONE SCREW 50mm 3J4MNE 09-Sep-2013 6.5 CANCELLOUS BONE SCREW 50mm 5V4MNE 11-Sep-2013 6.5 CANCELLOUS BONE SCREW 50mm MER715 18-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MER714 18-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MERDR9 23-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MERDRA 23-Nov-2013 6.5 CANCELLOUS BONE SCREW 50mm MERP11 05-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET0XY 07-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET27A 10-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET3M4 10-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET3M6 12-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm MET8YH 21-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm METE5N 21-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm METDV8 21-Dec-2013 6.5 CANCELLOUS BONE SCREW 50mm METNRN 04-Jan-2014 6.5 CANCELLOUS BONE SCREW 50mm METNRP 04-Jan-2014 6.5 CANCELLOUS BONE SCREW 50mm MHA0L5 11-Jan-2014 6.5 CANCELLOUS BONE SCREW 50mm MHA0MP 11-Jan-2014
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Worldwide Distribution
  • Product Description
    Stryker Orthopaedics Cancellous Bone Screw; || Dia 6.5 mm; Lnth: 50 mm; Sterile: || Made in the USA; || Stryker Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430. || The bone screws are optional fixtures that may be used during knee and hip replacement procedures.
  • 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