{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Stafford Springs",
      "state": "CT",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95577",
      "recalling_firm": "Hobbs Medical, Inc.",
      "address_1": "8 Spring St",
      "address_2": "N/A",
      "postal_code": "06076-1505",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of CT, GA, IN, MI, MN, MS, NH, NJ, NY, OH, TN, VT, WA, WI, WV and the country of Canada.",
      "recall_number": "Z-0470-2025",
      "product_description": "Posi-Stop Injection Needle, 23 Gauge, Catalog Number: 4706",
      "product_quantity": "6 units",
      "reason_for_recall": "Injection solutions would not flow as intended through the tip of 25ga-sized needles. Investigations that some units contained debris from the manufacturing process within the inner sheath that blocked the ID of the  needle.",
      "recall_initiation_date": "20241004",
      "center_classification_date": "20241115",
      "report_date": "20241127",
      "code_info": "Catalog Number: 4706; UDI-DI: M84947060; Lot Number: SD09-23-089."
    }
  ]
}