{
  "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": {
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      "status": "Ongoing",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90622",
      "recalling_firm": "Micro Therapeutics,  Inc.",
      "address_1": "9775 Toledo Way",
      "address_2": "",
      "postal_code": "92618-1811",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "US Nationwide Distribution: None  OUS: Brazil",
      "recall_number": "Z-1557-2022",
      "product_description": "Echelon -14 Micro Catheter, REF: 105-5092-150, sterile EO, Rx Only",
      "product_quantity": "2 units",
      "reason_for_recall": "Outer carton packaging of microcatheters were exposed to wet substance during transport.",
      "recall_initiation_date": "20220630",
      "center_classification_date": "20220818",
      "report_date": "20220824",
      "code_info": "Lot # B262322 UDI: (00) 847536005983",
      "more_code_info": ""
    }
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}