{
  "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": "Lexington",
      "address_1": "81 Hartwell Ave Ste 300",
      "reason_for_recall": "FUJIFILM has become aware that incorrect concentration values were printed on the bottle label for all product manufactured as part of Lot EL629. This may result incorrect results when used in testing.",
      "address_2": "",
      "product_quantity": "10 boxes (4 units per box)",
      "code_info": "Lot EL629, Model 990-28011",
      "center_classification_date": "20210128",
      "distribution_pattern": "US Nationwide distribution including in the states of MO, OR, MD, PA.",
      "state": "MA",
      "product_description": "Wako HDL-C/LDL-C Calibrator - Product Usage: designed to be used with Wako L-Type HDL-C or L-Type LDL-C for the determination of high density lipoprotein cholesterol (HDL-C) or low density lipoprotein cholesterol (LDL-C) in serum or plasma.",
      "report_date": "20210203",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Fujifilm Medical Systems U.S.A., Inc.",
      "recall_number": "Z-0932-2021",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "87098",
      "termination_date": "20210720",
      "more_code_info": "",
      "recall_initiation_date": "20201222",
      "postal_code": "02421-3160",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}