{
  "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": "63121",
      "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 (nationwide) and the countries of  AE, AR, AT, AU, BE, BR, CA,, CH,CL .CN, CO, CZ,DE, DK, EC, ES, FI, FR  GB, GP, GR, IE, IL, IN, IT, KR, LU, LY, MX, NC NL, NO, NZ, PE, PL  PT, RE, RU, SG, SI, TH, TN, TR, UG ,UY , VE, and ZA.",
      "recall_number": "Z-0151-2013",
      "product_description": "SpiraLok 6.5 w/out Needles with Orthocord  Product Number: 222971    SPIRALOK Anchors are primarily used to re-attach soft tissue to bone in rotator-cuff repair surgery, but are also indicated for use in the foot/ankle, knee and elbow",
      "product_quantity": "0",
      "reason_for_recall": "Fracture of SPIRALOK Anchors post op, requiring patient revision",
      "recall_initiation_date": "20120906",
      "center_classification_date": "20121025",
      "termination_date": "20150603",
      "report_date": "20121031",
      "code_info": "All lot codes"
    }
  ]
}