{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "West Chester",
      "address_1": "1301 Goshen Pkwy",
      "reason_for_recall": "Product incorrectly packaged.  The labels on the outside of the box and on the LCP Dia-Meta Volar Distal Radius Plate inside the box are correct; however, the preprinted box which contains the LCP-Dia-Meta Volar Distal Radius Plate is incorrect.  The box is preprinted for a 4.5 mm LCP Condylar Plate - Distal Femur.",
      "address_2": "",
      "product_quantity": "6 units",
      "code_info": "Lot Number 9890811, Catalog ID 02.110.115S",
      "center_classification_date": "20160610",
      "distribution_pattern": "Distributed to one customer: Colorado",
      "state": "PA",
      "product_description": "LCP Dia-Meta Volar Distal Radius Plate 15 H Shaft/LT-Sterile; Indicated for fractures, osteotomies, and non-unions of the radius and other small bones.",
      "report_date": "20160622",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Synthes (USA) Products LLC",
      "recall_number": "Z-1949-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "74082",
      "termination_date": "20161209",
      "more_code_info": "",
      "recall_initiation_date": "20160502",
      "postal_code": "19380-5986",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}