{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91220",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "",
      "postal_code": "02141-2289",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain,  Belgium, Canada, China, Croatia, Cura¿ao, Czechia, Denmark, Faroe Islands, Finland,  France, Germany, Hong Kong, Iceland, India, Iraq, Ireland, Israel, Italy, Japan, Jordan,  Kuwait, Latvia, Luxembourg, Malaysia, Netherlands, New Zealand, Norway, Oman, Portugal, Puerto Rico, Qatar, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia,  South Africa, Spain, Sri Lanka, Sweden, Switzerland, Tanzania, United Republic  Trinidad and Tabago, United Arab Emerates, United Kingdom.",
      "recall_number": "Z-0908-2023",
      "product_description": "Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor.  PN: 989803137631",
      "product_quantity": "69,679 cases (1,741,975 units)",
      "reason_for_recall": "Fetal Spiral Electrode (FSE) spiral tip of the FSE breaking off during use and requiring surgical intervention to remove the broken tip from the neonate patient. Philips has decided to discontinue the distribution of this product.",
      "recall_initiation_date": "20221121",
      "center_classification_date": "20230106",
      "report_date": "20230118",
      "code_info": "UDI: (01)20884838007431. All devices shipped to and received by the customer from Philips between May 2020 until end Nov 2022",
      "more_code_info": ""
    }
  ]
}