{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "325 Corporate Dr",
      "reason_for_recall": "Stryker received a report from the field indicating that a 5.5 mm Cancellous Bone Screw 40 mm was identified in packaging associated with a 6.5 mm Cancellous Bone Screw 25 mm.",
      "address_2": "",
      "product_quantity": "Catalog Number 2030-6525-1- 4 units; Catalog No: 2029-5540-1-7 units",
      "code_info": "1) 6.5 mm Cancellous Bone Screw 25mm  Catalog No: 2030-6525-1  Lot code MMLNLA    2) 5.5 Cancellous Bone Screw 40 mm  Catalog No: 2029-5540-1  Lot Code MMLMJ1",
      "center_classification_date": "20131211",
      "distribution_pattern": "Nationwide Distribution",
      "state": "NJ",
      "product_description": "Stryker Orthopaedics Cancellous Bone Screw  Howmedica Osteonics Corp.    Stryker France    Both the 6.4 mm diameter, 25mm length, Cancellous Bone Screws (Cat no 2030-6525-1) and the 5.5mm diameter, 40 mm length Cancellous Bone Screws (Cat no 2029-5540-1) are cleared for use in Total Hip Arthroplasty (THA), when implanting Stryker's Hemispherical Cluster Hole Acetabular Shell Systems and Total Knee Arthroplasty (TKA) when implanting Stryker's Series 7000 Standard Tibial Tray systems. The use of bone screws, during both THA and TKA are intended as supplemental fixation.",
      "report_date": "20131218",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Howmedica Osteonics Corp.",
      "recall_number": "Z-0483-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66908",
      "termination_date": "20150715",
      "more_code_info": "",
      "recall_initiation_date": "20131001",
      "postal_code": "07430-2002",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}