{
  "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": "2026-08-05",
    "results": {
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      "manufacturer_contact_zip_ext": "",
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          "manufacturer_d_name": "BECTON DICKINSON AND COMPANY",
          "manufacturer_d_address_1": "1 BECTON DRIVE",
          "manufacturer_d_address_2": "",
          "manufacturer_d_city": "FRANKLIN LAKES",
          "manufacturer_d_state": "NJ",
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          "manufacturer_d_country": "US",
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          "device_operator": "I",
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          "device_report_product_code": "FMI",
          "device_age_text": "1 YR",
          "device_evaluated_by_manufacturer": "",
          "combination_product_flag": "N",
          "udi_di": "",
          "udi_public": "",
          "openfda": {
            "device_name": "Needle, Hypodermic, Single Lumen",
            "medical_specialty_description": "General Hospital",
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      ],
      "product_problems": [
        "Fungus in Device Environment"
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      "reporter_state_code": "CA",
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      "suppl_dates_mfr_received": "",
      "mfr_report_type": "",
      "manufacturer_contact_country": "",
      "date_changed": "20250730",
      "health_professional": "",
      "summary_report_flag": "N",
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      "manufacturer_contact_extension": "",
      "manufacturer_city": "",
      "manufacturer_contact_phone_number": "",
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        {
          "patient_sequence_number": "1",
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          "patient_sex": "",
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          "patient_problems": [
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      "distributor_state": "",
      "event_key": "",
      "manufacturer_g1_country": "",
      "date_report_to_manufacturer": "20200427",
      "manufacturer_contact_city": "",
      "mdr_report_key": "10000339",
      "removal_correction_number": "",
      "number_devices_in_event": "",
      "date_report_to_fda": "20200422",
      "manufacturer_name": "",
      "report_source_code": "User Facility report",
      "remedial_action": [
        ""
      ],
      "manufacturer_g1_zip_code": "",
      "report_to_manufacturer": "",
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      "adverse_event_flag": "N",
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      "single_use_flag": "",
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      "mdr_text": [
        {
          "mdr_text_key": "189003043",
          "text_type_code": "Description of Event or Problem",
          "patient_sequence_number": "1",
          "text": "PER MD, \"WHEN I OPENED ONE OF OUR SEALED BD 30 GAUGE HALF INCH NEEDLES THIS MORNING, I NOTICED BLACK MOLD INSIDE THE NEEDLE.\" DEVICE RETAINED AND WILL BE RETURNED TO THE MANUFACTURER. NO PATIENT HARM; DEVICE WAS IDENTIFIED PRIOR TO USE ON A PATIENT."
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      ],
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      "manufacturer_contact_pcountry": "",
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    }
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}