{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "66190",
      "product_res_number": "Z-0581-2008",
      "event_date_initiated": "2007-11-21",
      "event_date_posted": "2008-02-22",
      "recall_status": "Terminated",
      "event_date_terminated": "2009-09-22",
      "res_event_number": "45807",
      "product_code": "KNC",
      "k_numbers": [
        "K915779"
      ],
      "product_description": "Hill-Rom Affinity Birthing Bed, Model P3600.",
      "code_info": "All units. (**Affinity beds manufactured with serial number I290AA7395 or greater are not impacted by this correction.)",
      "firm_fei_number": "1824206",
      "recalling_firm": "Hill-Rom, Inc.",
      "address_1": "125 E Pearl St",
      "city": "Batesville",
      "state": "IN",
      "postal_code": "47006",
      "additional_info_contact": "800-445-3730",
      "reason_for_recall": "Hole/opening on the labor bar -- Amputation of a finger could result, if a finger is placed into the opening, as the hole/opening creates a shear point when the mechanism is activated.",
      "root_cause_description": "Device Design",
      "action": "Consignees were notified of the problem via an Urgent Medical Device Correction letter dated 11/21/07.  Users were informed that they would be receiving a free upgrade kit for all of their Affinity Birthing Beds.  The Kit includes two plugs per bed, an insertion tool, and full written instructions.  An instruction video is available at www.Hill-Rom.com.",
      "product_quantity": "32,379 for all model numbers",
      "distribution_pattern": "Worldwide Distribution-- including USA and countries of Argentina, Australia, Austria, Bahamas, Bahrain, Belgium, Bermuda, Brazil, Brunei, Canada, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Dominican Republic, Egypt, Finland, France, Germany, Greece, Guam, Honduras, Hong Kong, Hungary, Iceland, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kuwait, Latvia, Lebanon, Malaysia, Mexico, Morocco, The Netherlands, New Calidonia, New Zealand, Nigeria, Northern Mariana Islands, Norway, Oman, Panama, Philippines, Poland, Portugal, Qatar, Republic of Korea, Saudi Arabia, Singapore, South Korea, Romania, Spain, Sweden, Switzerland, Taiwan, Thailand, Turkey, United Arab Emirates, United Kingdom, Uruguey, Venezuela, and Virgin Islands .",
      "openfda": {
        "k_number": [
          "K914544",
          "K831309",
          "K852171",
          "K861030",
          "K842962",
          "K862931",
          "K001261",
          "K924420",
          "K932035",
          "K903973",
          "K844183",
          "K870745",
          "K790950",
          "K820175",
          "K852174",
          "K830873",
          "K833321",
          "K792568",
          "K811902",
          "K770437",
          "K812141",
          "K831998",
          "K915779",
          "K864194",
          "K801622",
          "K884868"
        ],
        "device_name": "Table, Obstetric (And Accessories)",
        "medical_specialty_description": "Obstetrics/Gynecology",
        "regulation_number": "884.4900",
        "device_class": "2",
        "registration_number": [
          "1824206",
          "3007031002",
          "3007123908",
          "3040337865",
          "3033433849",
          "3006697241"
        ],
        "fei_number": [
          "1824206",
          "3007031002",
          "3007123908",
          "3040337865",
          "3033433849",
          "3006697241"
        ]
      }
    }
  ]
}