{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Portland",
      "state": "OR",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72451",
      "recalling_firm": "TZ Medical Inc.",
      "address_1": "17750 SW Upper Boones Ferry Rd Ste 150",
      "address_2": "N/A",
      "postal_code": "97224-7086",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution.",
      "recall_number": "Z-0293-2016",
      "product_description": "Neptune Plus, HEMOSTASIS PAD WITH ANTIMICROBIAL BARRIER, For hemostasis following needle/sheath removal, Part number 8870-03",
      "product_quantity": "32,170 units",
      "reason_for_recall": "The IFU of the Neptune Plus Pads, does not match that submitted in the original 510k.  Need to remove: for haemostasis following needle/sheath removal",
      "recall_initiation_date": "20151014",
      "center_classification_date": "20151118",
      "termination_date": "20161024",
      "report_date": "20151125",
      "code_info": "Lot Numbers:    AGR554;  AGR554\\20;  AGR554\\24;  AGR554/24;  AGR570\\28;  AGR570/43;  AGR744124;  AGR744137."
    }
  ]
}