{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Completed",
      "city": "Campbell",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88611",
      "recalling_firm": "IMPERATIVE CARE INC",
      "address_1": "1359 Dell Ave",
      "address_2": "N/A",
      "postal_code": "95008-6609",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution.",
      "recall_number": "Z-2577-2021",
      "product_description": "Imperative Care, ZOOM 71 Reperfusion Catheter, REF: ICRC071137,  TRX Tip, 137 cm, 6F (.083 in/2.11 mm), .071 in/1.8 mm), STERILE.EO, Rx Only, UDI: (01) 00812212030191.  For neurovascular procedures.",
      "product_quantity": "3118 units",
      "reason_for_recall": "There is a potential for distal end of catheters to fracture and become detached.",
      "recall_initiation_date": "20210813",
      "center_classification_date": "20210929",
      "report_date": "20211006",
      "code_info": "Affected Lots:  V2014902, F2026201, F2026802, F2028801, F2028901, F2029501, F2029701, F2030801, F2031101, F2035301, F2032502, F2100802, F2101301, F2104102, F2108101, F2108801, F2109601, F2109701, F2111101, F2110601, F2112301, F2113004, F2112001"
    }
  ]
}