{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82927",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "15 Hampshire St Bldg 5",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide  Foreign: AU, BE, CA, DK, FI, GB, IE, NL",
      "recall_number": "Z-2038-2019",
      "product_description": "Monoject Standard Hypodermic Needle, 16 G x 1-1/2\"  Item code: 8881200037",
      "product_quantity": "N/A",
      "reason_for_recall": "Manufacturing defect was found for the cartridge component, which could compromise the sterility barrier of the product",
      "recall_initiation_date": "20190430",
      "center_classification_date": "20190723",
      "report_date": "20190731",
      "code_info": "Lot Number:904212, 905612, 907002"
    }
  ]
}