{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72205",
      "recalling_firm": "Smith & Nephew, Inc., Endoscopy Div.",
      "address_1": "130 Forbes Blvd",
      "address_2": "N/A",
      "postal_code": "02048",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US Nationwide, Canada, Austria, Australia, Belgium, China,  Spain, Finland, France, Great Britain, Greece, Germany, Hungary, India, Italy, Japan, Korea, Lithuania,  Latvia,  Netherlands, Poland, Portugal, Sweden, Thailand, Turkey, Ukraine and Venezuela",
      "recall_number": "Z-0156-2016",
      "product_description": "Smith & Nephew MOSAICPLASTY DP- Disposable Harvesting System 4.5 mm, Sterile  Part Number:  7209235    Intended Use: For arthroscopic (knee and ankle) and open osteochondral grafting fix for osteochondral (cartilage) defects.",
      "product_quantity": "1287 units",
      "reason_for_recall": "Sterility of device is compromised due to breach in the packaging",
      "recall_initiation_date": "20150910",
      "center_classification_date": "20151022",
      "termination_date": "20210623",
      "report_date": "20151028",
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}