{
  "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": [
    {
      "country": "United States",
      "city": "Bloomington",
      "address_1": "3895 W Vernal Pike",
      "reason_for_recall": "Customer contacted Biomedix of complaint and returned the failed set along with 86 units of unopened stock (96 units originally shipped).  Biomedix performed extensive investigation and found insufficient application of glue.  Recall was initiated due to the rate of the failure.",
      "address_2": "",
      "product_quantity": "2,928",
      "code_info": "Model/Product Number:  B30-102    Lot #416130    Exp. 12/2016",
      "center_classification_date": "20141006",
      "distribution_pattern": "US Distribution including the states of OH, NC, and TX",
      "state": "IN",
      "product_description": "Biomedix SELEC-3 I.V. Administration Set.  Individually sealed into a Tyvek¿ and LDPE/PET pouch.  Secondary packaging includes 48 pouched units per box/case.  STERILE",
      "report_date": "20141015",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Biomedix, Inc.",
      "recall_number": "Z-0023-2015",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "69249",
      "termination_date": "20141113",
      "more_code_info": "",
      "recall_initiation_date": "20140814",
      "postal_code": "47404-2533",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}