{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Batesville",
      "address_1": "1069 State Road 46 E",
      "reason_for_recall": "Complaints (including one reported death) allegedly of the lift arm drifting down suddenly.  If the lift arm assembly is manually lifted, the actuator can become damaged and get stuck in the highest position.  If a patient is lifted into the sling while the actuator is stuck, there is a potential risk of a free fall of the patient, resulting in minor or potentially catastrophic injuries.",
      "address_2": "",
      "product_quantity": "24, 798",
      "code_info": "Viking¿ M Lift  \u0010 Model 2040035 (S/N 9 200 000 - 9 201 689)  \u0010 Model 2040015 (S/N 7 500 401 - 7 568 899)  \u0010 Model 2040005 (S/N 7 100 101 - 7 200 200)  Viking¿ L Lift  \u0010 Model 2040004 (S/N 7 200 201 - 7 300 300)  Viking¿ XL/Viking¿ 300 Lift  \u0010 Model 2040003 (S/N 800 001 - 804 999)",
      "center_classification_date": "20150618",
      "distribution_pattern": "Worldwide Distribution -- AE, AO, AR, AT, AU, AZ, BD, BE, BG, BH, BR, CA, CH, CL, CN, CO, CS, CZ, DE, DK, EG, ES, FI, FR, GR, HK, HR, HU, ID, IE, IL, IN, IQ, IR, IS, IT, JO, JP, KR, KW, LB, LI, LT, LU, LV, MA, MT, MX, MY, NL, NO, NZ, OM, PH, PL, PT, QA, RO, SA, SE, SG, SI, SK, SY, TH, TN, TR, TW, UK, US, VE, and ZA.",
      "state": "IN",
      "product_description": "Viking M, L, and XL Mobile Lifts.    Non-AC-powered patient lift.",
      "report_date": "20150624",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Hill-Rom, Inc.",
      "recall_number": "Z-1818-2015",
      "initial_firm_notification": "",
      "product_type": "Devices",
      "event_id": "71132",
      "termination_date": "20170804",
      "more_code_info": "",
      "recall_initiation_date": "20150320",
      "postal_code": "47006-7520",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}