{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "53251",
      "product_res_number": "Z-0240-2008",
      "event_date_initiated": "2006-11-12",
      "event_date_posted": "2007-07-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-10-22",
      "res_event_number": "38256",
      "product_code": "FIN",
      "product_description": "Hill-Rom VersaCare Hospital Bed System; Models P3200 and P3201, Hill-Rom, Batesville, IN 47006",
      "code_info": "Serial numbers E322AD0046 through H023AD6179. (E means 2003 production, F means 2004 production, G means 2005 production and H means 2006 production).",
      "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": "812-934-7777",
      "reason_for_recall": "False Latch/Failure to Latch-The side rail may not latch, or the latch may not fully engage, resulting in the siderail being able to be lowered without pulling on the release handle.",
      "root_cause_description": "Device Design",
      "action": "The firm notified consignees via an Urgent Device Correction letter dated 11/12/07 informing them of the problem and informed them they would be receiving upgrade kits which they could have their qualified personnel install themselves following video instructions also provided, or they could contact Hill-Rom for assistance.",
      "product_quantity": "43,731 beds total for both models were distributed; 3,282 have been corrected to date.",
      "distribution_pattern": "Worldwide, including USA, Argentina, Australia, Brazil, Canada, Dominican Republic, Emirate of Sharjah, England, Greece, Indonesia, Japan, Jordan, Kuwait, Lebanon, Malaysia, Mexico, Oman, Pakistan, Philippines, Qatar, Saudi Arabia, Selangor, Singapore, South Korea, Spain, Taiwan, Thailand, Turkey, United Arab Emirates and Venezuela.",
      "openfda": {
        "k_number": [
          "K003560",
          "K140984",
          "K112427",
          "K023011",
          "K093641",
          "K873166",
          "K031502",
          "K993058",
          "K961416",
          "K970674",
          "K883408",
          "K993272",
          "K060333",
          "K141213",
          "K992793",
          "K033118",
          "K030366",
          "K051031"
        ],
        "device_name": "Tank, Holding, Dialysis",
        "medical_specialty_description": "Gastroenterology, Urology",
        "regulation_number": "876.5820",
        "device_class": "2",
        "registration_number": [
          "3019131",
          "1055109",
          "3003768032",
          "1530185",
          "3005021818"
        ],
        "fei_number": [
          "1000515504",
          "3006475063",
          "3013942511",
          "3005021818",
          "1000112932"
        ]
      }
    }
  ]
}