{
  "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": "Austin",
      "address_1": "9800 Metric Blvd",
      "reason_for_recall": "One lot of the 010-55-030, 6.5 mm Cancellous Bone Screw was recalled because a product complaint identified a mislabeling of the device.  Although the package label indicates Size 30mm, the screw dimension is actually 25mm.",
      "address_2": "",
      "product_quantity": "18 devices",
      "code_info": "Lot 007A1037, Ref 010-55-25.",
      "center_classification_date": "20120806",
      "distribution_pattern": "Nationwide Distribution including AR, CA, FL, ID, OK, PA, TX, and UT.",
      "state": "TX",
      "product_description": "djo surgical Screw 6.5 mm, Sz 25mm, low profile.    Product is intended for the fixation of the acetabular shell or fracture repair",
      "report_date": "20120815",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Encore Medical, Lp",
      "recall_number": "Z-2146-2012",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "62561",
      "termination_date": "20121204",
      "more_code_info": "",
      "recall_initiation_date": "20120716",
      "postal_code": "78758",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}