{
  "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": "Terminated",
      "city": "Springfield",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89680",
      "recalling_firm": "DRG International, Inc.",
      "address_1": "841 Mountain Ave",
      "address_2": "",
      "postal_code": "07081-3437",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "NY",
      "recall_number": "Z-0896-2022",
      "product_description": "C-Peptide ELISA : IVD measurement of C-Peptide in serum, plasma (EDTA-, heparin- or citrate plasma) and urine. Catalog # EIA-1293",
      "product_quantity": "3 Kits",
      "reason_for_recall": "ODs of the standards too low(< 0.6 ODmax) may cause invalid runs, delayed patient results are possible",
      "recall_initiation_date": "20211221",
      "center_classification_date": "20220407",
      "termination_date": "20240212",
      "report_date": "20220413",
      "code_info": "Lot# / Expiration dates:   20K061 / 2022-06-30 20K071 / 2022-07-31 20K081 / 2022-08-31",
      "more_code_info": ""
    }
  ]
}