{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "197270",
      "product_res_number": "Z-0908-2023",
      "event_date_initiated": "2022-11-21",
      "event_date_posted": "2023-01-06",
      "recall_status": "Open, Classified",
      "res_event_number": "91220",
      "product_code": "HGP",
      "k_numbers": [
        "K030691"
      ],
      "product_description": "Philips Fetal Spiral Electrode-intended for patients requiring fetal heart rate monitoring during labor.\nPN: 989803137631",
      "code_info": "UDI: (01)20884838007431.\nAll devices shipped to and received by the customer from Philips between May 2020 until end Nov 2022",
      "firm_fei_number": "3016618143",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "city": "Cambridge",
      "state": "MA",
      "postal_code": "02141-2289",
      "additional_info_contact": "Philips Customer Services\n800-722-9377",
      "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.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Philips Medical issued to U.S. customers, the Urgent Medical Device Correction (UMDC) letter via certified mail 11/21/22. Philips Market Organizations are responsible for distributing the letters outside of the U.S. Letter states reason for recall, health risk and action to take. Philips has decided to discontinue the distribution of this product.\nTo limit the potential for the spiral tip of the FSE to break off in the patient s scalp, it is important to avoid over rotation during attachment or pulling the tip from the fetal scalp\n\n Customer should complete the Urgent Field Safety Notice Response Form online to submit both their acknowledgement of this recall (mandatory) and actions taken, as well as request for credit (optional). To request credit go to URL: https://forms.office.com/r/GsLVh2gYZi\nPass this notice to all those who need to be aware within your organization or to any organization where the potentially affected devices have been transferred. (If appropriate).\nIf you choose, discard all FSEs sold by Philips and source from an alternative supplier available in your country. If you choose to discard the FSEs, we will issue a credit after you complete the online response form.\n\nActions planned by Philips Hospital Patient Monitoring to correct the problem\n\" Philips is continuing to investigate additional root causes with FSE supplier\n\" Philips will immediately discontinue selling the FSEs\n\" Philips will reimburse for any discarded FSEs",
      "product_quantity": "69,679 cases (1,741,975 units)",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Australia, Austria, Bahrain, \nBelgium, Canada, China, Croatia, Cura¿ao, Czechia, Denmark, Faroe Islands, Finland, \nFrance, Germany, Hong Kong, Iceland, India, Iraq, Ireland, Israel, Italy, Japan, Jordan, \nKuwait, Latvia, Luxembourg, Malaysia, Netherlands, New Zealand, Norway, Oman, Portugal, Puerto Rico, Qatar, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, \nSouth Africa, Spain, Sri Lanka, Sweden, Switzerland, Tanzania, United Republic \nTrinidad and Tabago, United Arab Emerates, United Kingdom.",
      "openfda": {
        "k_number": [
          "K872057",
          "K901152",
          "K943732",
          "K911657",
          "K771553",
          "K844608",
          "K910815",
          "K871079",
          "K801984",
          "K003458",
          "K030691",
          "K904745",
          "K905830",
          "K822584",
          "K905130",
          "K243291",
          "K792669"
        ],
        "registration_number": [
          "1720929",
          "1000576299",
          "1066270",
          "3010838917",
          "3000126629",
          "1423537",
          "2032098",
          "3006695553",
          "9610632",
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        ],
        "fei_number": [
          "1720929",
          "1000576299",
          "3000957797",
          "3010838917",
          "1000220650",
          "3000126629",
          "3003058448",
          "3006695553",
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          "3003678543",
          "3001236905",
          "3004729605",
          "3002808022",
          "3002808026",
          "3016618143"
        ],
        "device_name": "Electrode, Circular (Spiral), Scalp And Applicator",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.2675",
        "device_class": "2"
      }
    }
  ]
}