{
  "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": [
    {
      "status": "Terminated",
      "city": "Raynham",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64913",
      "recalling_firm": "DePuy Mitek, Inc., a Johnson & Johnson Co.",
      "address_1": "325 Paramount Drive",
      "address_2": "N/A",
      "postal_code": "02767-5199",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA including KY, NJ and Internationally to Argnetina, Australia,  Belgium,Columbia, India, France, Japan, Jordan, Latvija,  Israel,  Korea,  and Great Britain.  For questions regarding this recall call 508-977-3813.",
      "recall_number": "Z-1278-2013",
      "product_description": "DePuy Mitek Tissue Liberator -Blade Up  Catalog Number:  214623    The Reusable Arthroscopy Instruments are reusable, non-powered surgical instruments used during arthroscopic surgery of any joint except the spine.",
      "product_quantity": "27 units",
      "reason_for_recall": "Labeled incorrectly as a Blade Up configuration instead of a Blade Down configuration.",
      "recall_initiation_date": "20130415",
      "center_classification_date": "20130509",
      "termination_date": "20160311",
      "report_date": "20130515",
      "code_info": "Lot number:13A01"
    }
  ]
}