{
  "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": "49,074 devices",
      "code_info": "UDI: (01)10385609020039(17)XXXXXX(10)XXXXXXXX    Lot Numbers:  DM218001  DM218002  DM218003  DM218004  DM218005  DM218006  DM218020  DM218025  DM218034  DM218035    DM218036",
      "center_classification_date": "20191026",
      "distribution_pattern": "Nationwide within U.S.",
      "state": "MA",
      "product_description": "DEMO No Needle Corrugated Carton 20 U/D, Part Number 2260-03",
      "report_date": "20191106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Valeritas, Incorporated",
      "recall_number": "Z-0195-2020",
      "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"
    }
  ]
}