{
  "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": "Franklin",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69723",
      "recalling_firm": "Arthrosurface, Inc.",
      "address_1": "28 Forge Pkwy",
      "address_2": "N/A",
      "postal_code": "02038",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - USA nationwide.  Internationally distributed to Europe, Canada, and Australia.  Only products in US affected by this recall.",
      "recall_number": "Z-1110-2015",
      "product_description": "Arthrosurface 25&30mm 10.5x28mm Taper Post Fixation Component; Catalog Number: 6105-0028, Pat Number 1105-0028.   HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing.  Orthopedic shoulder prosthesis component.",
      "product_quantity": "136",
      "reason_for_recall": "Fully threaded Taper Post Fixation components not cleared for marketing in the US with current indications.",
      "recall_initiation_date": "20141124",
      "center_classification_date": "20150212",
      "termination_date": "20150327",
      "report_date": "20150218",
      "code_info": "Catalog Number: 6105-0028, Part Number 1105-0028"
    }
  ]
}