{
  "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": "Indianapolis",
      "address_1": "9115 Hague Rd",
      "reason_for_recall": "Internal Roche inspections have revealed that after the lancet is used for a finger stick, the needle may not fully retract back within the lancet drum or back into the cap. This allows the needle to protrude inside the cap or outside of the cap of the ACCU-CHEK FastClix lancing device.",
      "address_2": "",
      "product_quantity": "36,332",
      "code_info": "Lot Number(s):  GDA 048, GDA050, GDA 051, GDA 063",
      "center_classification_date": "20130828",
      "distribution_pattern": "Nationwide Distribution",
      "state": "IN",
      "product_description": "ACCU-CHECK FastClix Lancing Device. It is intended for use in conjunction with a blood glucose monitoring system.",
      "report_date": "20130904",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Roche Diagnostics Operations, Inc.",
      "recall_number": "Z-2109-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "65886",
      "termination_date": "20140512",
      "more_code_info": "",
      "recall_initiation_date": "20130819",
      "postal_code": "46256-1025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}