{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Warrendale",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92136",
      "recalling_firm": "OmniCell, Inc.",
      "address_1": "51 Pennwood Pl Ste 400",
      "address_2": "N/A",
      "postal_code": "15086-6506",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "AL, NY",
      "recall_number": "Z-1617-2023",
      "product_description": "Omnicell IVX Station-For use in the automated preparation of pharmaceutical admixtures and syringes  Model Number: 298921373",
      "product_quantity": "6 units",
      "reason_for_recall": "IVX Station does not account for inherent scale inaccuracy or variability, could result in a preparation being passed that is outside of the dose accuracy stated in the product labeling",
      "recall_initiation_date": "20230327",
      "center_classification_date": "20230522",
      "report_date": "20230531",
      "code_info": "UDI-DI: 00860006285005 Serial Numbers:  IVXS000014, IVXS000015, IVXS000016, IVXS000017, IVXS000018. IVXS000019"
    }
  ]
}