{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98168",
      "recalling_firm": "ICU Medical Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, FL, IL, IN, MA, MI, MN, MO, NE, NJ, NY, OH,  OK, TX, WA.",
      "recall_number": "Z-1101-2026",
      "product_description": "Portex Spinal Tray, Item No. A3729-24  A3595",
      "product_quantity": "64290 total",
      "reason_for_recall": "Affected lots of syringes may have a crack on the syringe collar, which may lead to delayed or repeated blood draw/fluid delivery. This issue may also lead to blood leakage during sampling of arterial blood or leakage during fluid delivery.",
      "recall_initiation_date": "20251219",
      "center_classification_date": "20260115",
      "report_date": "20260121",
      "code_info": "1. A3729-24 UDI-DI 30351688075691 Lots 6146204 (corrected on 1/22/26, removed \"-LSM\" suffix.  2. A3595 UDI-DI 35019517108211 Lot 6157980",
      "more_code_info": ""
    }
  ]
}