{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Maryland Heights",
      "address_1": "10888 Metro Ct",
      "reason_for_recall": "Premature strap wear and breakage at maximum weight conditions (625 lbs.).",
      "address_2": "",
      "product_quantity": "716",
      "code_info": "Device Model; 323100, 323102, 323117, 323118, 323120, 323137, 323149, 323150, 323215, 323225, 323237, 323240, 323400, 323417, 323450, 323600, 323602, 323700, 323750, 323840, 323851, 323917, 323117V, and 323150V",
      "center_classification_date": "20180820",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of AK, CA, CT, DE, GA, IA, IL, KY, LA, MA, ME, MI, MN, MO, NE, NV, NY, OH, OR, PA, RI, TN, TX, WI, and Puerto Rico and the countries of Canada and Australia,",
      "state": "MO",
      "product_description": "Handicare C Series Patient Lift    Product Usage:  A device used to lift and transport a patient from one place to another.",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Handicare Usa Inc",
      "recall_number": "Z-2752-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80556",
      "termination_date": "20200710",
      "more_code_info": "",
      "recall_initiation_date": "20171103",
      "postal_code": "63043-2413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}