{
  "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": "2026-04-01",
    "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": "85981",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "150 Minuteman Rd",
      "address_2": "",
      "postal_code": "01810-1031",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Domestic distribution to AL  AR  AZ  CO  GA  IL  IN  KS  KY  MD  MN  MO  NC  NE  NJ  NY  OK  PA  PR  TN  TX  VA  WI. Foreign distribution to Australia  Austria  Belgium  Finland  France  Germany  Great Britain  Ireland  Italy  Japan  Luxembourg  Mexico  Netherlands  Poland  Portugal  Singapore  South Africa  Spain  Sweden  Switzerland",
      "recall_number": "Z-2746-2020",
      "product_description": "SUTUREFIX ULTRA Suture, Product number 72203855",
      "product_quantity": "868",
      "reason_for_recall": "A packaging error resulted in a XL drill being presented for use instead of the S drill. The XL drill is one inch longer than the S drill.",
      "recall_initiation_date": "20200624",
      "center_classification_date": "20200731",
      "report_date": "20200812",
      "code_info": "Lot numbers 2038366, 2039311 and 2046505",
      "more_code_info": ""
    }
  ]
}