{
  "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": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85296",
      "recalling_firm": "Smith & Nephew, Inc.",
      "address_1": "130 & 120 Forbes Blvd",
      "address_2": "N/A",
      "postal_code": "02048",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide  Foreign:  AE  AL  AR  AT  AU  BE  BM  BR  CA  CH  CL  CN  CO  CR  CZ  DE  DK  EC  EE  ES  FI  FR  GB  IE  IL  IN  IT  KR  LT  LV  MT  MX  NO  PA  PE  PL  PR  PT  QA  RU  SE  SG  TH  TR  XK  ZA",
      "recall_number": "Z-1756-2020",
      "product_description": "Smith & Nephew FOOTPRINT ULTRA PK SUTURE ANCHOR 4.5  Part Number: 72202901",
      "product_quantity": "125,196 (total)",
      "reason_for_recall": "Space between the device and the packaging permits excessive movement which could potentially lead to the displacement of the anchors tip protector allowing the tip of the anchor to create a sterile breach.",
      "recall_initiation_date": "20200317",
      "center_classification_date": "20200422",
      "report_date": "20200429",
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