{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95524",
      "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.",
      "recall_number": "Z-0561-2025",
      "product_description": "Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp,  Part Number 5C4482S; use in Peritoneal Dialysis",
      "product_quantity": "31248 units",
      "reason_for_recall": "There has been an increase in the number of complaints related to the separation of the female connector from the main body of the transfer set.",
      "recall_initiation_date": "20241023",
      "center_classification_date": "20241127",
      "report_date": "20241204",
      "code_info": "UDI/DI 00085412476261, Lot/Serial Numbers:  H23J13063, H23J26081, H24B18059, H24B19065, H24B19099, H24B20071, H24C18065, H24E22062, H24F11048",
      "more_code_info": ""
    }
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}