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.
Stryker spine received reports of packaging failures during shipping for the jam shidi instruments, which may compromise the sterility of the product.
조치
Stryker Spine issued an "Urgent Product Recall" notification dated January 15, 2010 via Federal Express to all consignees. The letter informed users of the issue and potential hazards of the affected product.
For further information, contact your local Stryker Spine Sales Representative or call 201-760-8206.
Stryker Xia Precision System; Jam Shidi 11 Gauge 5 inch; Sterile; Manufactured for: Stryker Spine SAS, Cestas, France; Distributed in the US by Howmedica Osteonics Corp, 325 Corporate Drive, Mahwah, NJ. || Intended for use as a manual surgical instrument during percutaneous posterior, non-cervical pedicle fixation.