{
  "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": "Kalona",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80656",
      "recalling_firm": "Civco Medical Instruments Co. Inc.",
      "address_1": "102 1st St S",
      "address_2": "N/A",
      "postal_code": "52247-9589",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "United States, Austria, Belgium, Denmark, France, Germany, Poland, Spain, Switzerland and United Kingdom",
      "recall_number": "Z-2947-2018",
      "product_description": "CIVCO Needle Guide, REF 676-150, QTY 24, STERILE EO",
      "product_quantity": "3 units",
      "reason_for_recall": "The assembly of the needle guides were found to be either missing adhesive or did not have adequate adhesive to hold the assembled cannula in place on the needle guide.",
      "recall_initiation_date": "20180730",
      "center_classification_date": "20180829",
      "termination_date": "20200916",
      "report_date": "20180905",
      "code_info": "UDI 00841436107334, Lot numbers:  A035054, A042207"
    }
  ]
}