{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "country": "United States",
      "city": "Vancouver",
      "address_1": "1801 W Fourth Plain Blvd",
      "reason_for_recall": "The firm had received a complaint alleging that a medical professional had difficulty inserting a guide wire into a needle",
      "address_2": "",
      "product_quantity": "1100 pieces",
      "code_info": "Lot 9184-A",
      "center_classification_date": "20151201",
      "distribution_pattern": "Distributed in the states of MT and NY.",
      "state": "WA",
      "product_description": "U-SDN 2 Part Ultra Modified Seldinger Needles, NS/37-0387.    All needles were sold in bulk, non-sterile, and intended for further processing. Needles are packaged in zipper-bags, 300 pieces per bag, with shipment occurring in a corrugated cardboard box. Needles consist of a stainless steel cannula with a molded plastic hub. This needle is intended to be placed over the guidewire to enlarge the opening in the vessel.  Vessel dilator, for percutaneous catheterization.",
      "report_date": "20151209",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Procedure Products, Inc.",
      "recall_number": "Z-0355-2016",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "72596",
      "termination_date": "20160401",
      "more_code_info": "",
      "recall_initiation_date": "20151027",
      "postal_code": "98660-1310",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}