{
  "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": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90658",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide) distribution and OUS (foreign) : Australia, Finland, Germany, Spain and United Kingdom.",
      "recall_number": "Z-1577-2022",
      "product_description": "Baxter DISCPAC Syringe Tip Caps, Self-Righting, Luer Slip, White REF H938671100",
      "product_quantity": "10140 units",
      "reason_for_recall": "There is a potential of the packaging not maintaining a sterile barrier for the tip caps.",
      "recall_initiation_date": "20220722",
      "center_classification_date": "20220825",
      "report_date": "20220831",
      "code_info": "REF H938671100, UDI 00085412479750",
      "more_code_info": ""
    }
  ]
}