{
  "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": "2026-06-24",
    "results": {
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      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98306",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "States: Ohio  Countries: United States",
      "recall_number": "Z-1368-2026",
      "product_description": "Brand Name: Spectrum IQ  Product Name: Infusion Pump  Model/Catalog Number: 3570009  Software Version: N/A  Product Description: Infusion Pump, one unit per carton  Component: N/A",
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      "reason_for_recall": "Pumps were released without full testing being performed, including occlusion alarm testing.",
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      "center_classification_date": "20260213",
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      "code_info": "Lot Code: GTIN 00085412610900, Serial Numbers 3815663, 3823468, 3824743, 3825234, and 3825599",
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