{
  "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": [
    {
      "country": "United States",
      "city": "Marlborough",
      "address_1": "293 Boston Post Rd W Ste 330",
      "reason_for_recall": "There is a potential for \"No Needle Demo Units\" to contain a needle.",
      "address_2": "",
      "product_quantity": "21,714 devices",
      "code_info": "UDI:  (01)10385609020015(17)XXXXXX(10)XXXXXXXX    Lot Numbers:  DM418011  DM418012  DM418013   DM418014  DM418015  DM418016  DM418017  DM418031  DM418033  DM418037",
      "center_classification_date": "20191026",
      "distribution_pattern": "Nationwide within U.S.",
      "state": "MA",
      "product_description": "DEMO No Needle Corrugated Carton 40 U/D, Part Number 2260-01",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Valeritas, Incorporated",
      "recall_number": "Z-0197-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83386",
      "termination_date": "20200624",
      "more_code_info": "",
      "recall_initiation_date": "20190703",
      "postal_code": "01752-4615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}