{
  "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": "Totowa",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63481",
      "recalling_firm": "Vital Signs Devices, a GE Healthcare Company",
      "address_1": "20 Campus Rd",
      "address_2": "N/A",
      "postal_code": "07512-1210",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) including states:  AZ, CA, CT, FL, GA, IL, KS, KY, MA, MD, MN, MO, NJ, NM, NY, OH, PA, SC,TX, WA, and WY; and countries of: Australia and Canada.",
      "recall_number": "Z-0330-2013",
      "product_description": "Corometrics Qwik Connect Plus Spiral Electrode- Model #7000AA0      A fetal scalp circular (spiral) electrode and applicator is a device used to obtain a fetal electrocardiogram during labor and delivery.",
      "product_quantity": "126 cases (50 pouches per case)",
      "reason_for_recall": "Thirty fetal scalp electrodes were found to have an incomplete package seal and lacked the printed lot number stamped on during sealing.",
      "recall_initiation_date": "20121016",
      "center_classification_date": "20121116",
      "termination_date": "20140416",
      "report_date": "20121128",
      "code_info": "Lot #S03123  Model #7000AA0"
    }
  ]
}