{
  "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-1113-2015",
      "product_description": "Athrosurface 40mm 13.75x31mm Taper Post Fixation Component; Catalog Number:  8135-1875 Part Number: 3135-1875.   HemiCAP Contoured Articular Prosthetic for Humeral head resurfacing.  Orthopedic shoulder prosthesis component.",
      "product_quantity": "182 units",
      "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:  8135-1875 Part Number: 3135-1875"
    }
  ]
}