{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95654",
      "recalling_firm": "Smith & Nephew Inc.",
      "address_1": "150 Minuteman Rd",
      "address_2": "",
      "postal_code": "01810-1031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AK, AL, IL, IN, KY, MD, MN, NC, NE, NH, NJ, TX and the countries of CA, CL, CN, EC, ES, GB, KZ, NO, PE, PL, RU, TR.",
      "recall_number": "Z-0581-2025",
      "product_description": "BIORAPTOR Suture Anchors. Tendon/ligament, non-bioabsorbable bone anchor.",
      "product_quantity": "2,156 units",
      "reason_for_recall": "Sterile barrier breach due to inadequate packaging design that could not hold the geometry of the device.",
      "recall_initiation_date": "20241029",
      "center_classification_date": "20241129",
      "report_date": "20241211",
      "code_info": "Part No. 72201541, 72201542, 72203280, 72203281; UDI-DI: 03596010595072, 03596010595089, 03596010656452, 03596010656469; Batch No. 2146369, 2151242, 2151690, 2154691, 2153489, 2151692.",
      "more_code_info": ""
    }
  ]
}