{
  "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": "Milan",
      "state": "",
      "country": "Italy",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88680",
      "recalling_firm": "Sentinel CH SpA",
      "address_1": "Via Robert Koch 2",
      "address_2": "",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US Nationwide distribution in the states of LA, MD, MN, ND, NY, WV, and Puerto Rico.",
      "recall_number": "Z-0033-2022",
      "product_description": "Alinity c CRP Vario Cardiac High Sensitivity Calibrator Kit (ref 07P5605) - Product Usage: use in the calibration of the Alinity c CRP Vario assay, Cardiac CRP high sensitivity method [Cardiac CRP], on the Alinity c analyzer.",
      "product_quantity": "32",
      "reason_for_recall": "Calibrator vials were incorrectly labeled. Use of incorrectly labeled vials will cause the instrument to generate a warning that calibrators are incorrectly loaded and calibration will not be completed successfully.",
      "recall_initiation_date": "20210729",
      "center_classification_date": "20211006",
      "termination_date": "20230724",
      "report_date": "20211013",
      "code_info": "Lot 00681Y600",
      "more_code_info": ""
    }
  ]
}