{
  "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": "2026-04-29",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Kalona",
      "state": "IA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98513",
      "recalling_firm": "Civco Medical Instruments Co. Inc.",
      "address_1": "102 1st St S",
      "address_2": "",
      "postal_code": "52247-9589",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "",
      "distribution_pattern": "US States: OH, PA, WA. China.",
      "recall_number": "Z-1734-2026",
      "product_description": "eTRAX Needle System Starter Kit 18G (for Aurora Trackers), Part Number 667-152",
      "product_quantity": "20 units",
      "reason_for_recall": "There was an error in inspection and programming of the eTRAX needle sensor for Aurora trackers. The result is a potential for the needle tip position to be incorrectly identified on the user interface.",
      "recall_initiation_date": "20260302",
      "center_classification_date": "20260401",
      "report_date": "20260408",
      "code_info": "UDI-DI: 00841436111065; Lot Number: A233347, A228677, A268116, A268238, A272513, A279457, A280388 , A281840",
      "more_code_info": ""
    }
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}