{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77402",
      "recalling_firm": "Smiths Medical ASD Inc.",
      "address_1": "6000 Nathan Ln N",
      "address_2": "N/A",
      "postal_code": "55442-1690",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the state of : IN",
      "recall_number": "Z-2670-2017",
      "product_description": "Jelco, Hypodermic needle Pro¿ needles 19G X1 1/2\" 800/CA Model No.  EL 1915 & 19G X 2\" 600/CA Model No. SB 5021, Rx Only, Sterile EO.",
      "product_quantity": "736,000",
      "reason_for_recall": "Smiths Medical became aware on January 11, 2017, that syringe assemblies provided by Nipro Medical Corporation contained pin holes in the side wall of the hub. The defect was not detected during Smiths Medical incoming inspection. The syringe assemblies were used to manufacture seven (7) finished good lots of Hypodermic Needle Pro¿ needles, Smiths Medical part numbers EL 1915 and SB5021.",
      "recall_initiation_date": "20170404",
      "center_classification_date": "20170703",
      "termination_date": "20190805",
      "report_date": "20170712",
      "code_info": "3297460,3297461 Model No. EL1915.    3297458,3297459,3297465,  3297466,3297467 Model No. SB5021."
    }
  ]
}