{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96856",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide",
      "recall_number": "Z-2032-2025",
      "product_description": "Hillrom LikoScale component, Product Code 3156232,  used with the following adapter kits for patient lifts:    1) LikoScale 200 Accessory - Product Code 3156225;   2) LikoScale 350 Accessory - Product Code 3156228;   3)  LikoScale 400 Accessory - Product Code 3156226.",
      "product_quantity": "9839 units",
      "reason_for_recall": "The Q-link 13 could allow for an improper attachment (false latching) of the Quick-Release Hook used on Sling Bars and other accessories. This could result in a critical injury from a patient fall as the false latched component may initially bear weight but can loosen from the Q-link resulting in a detachment and drop.",
      "recall_initiation_date": "20250530",
      "center_classification_date": "20250709",
      "report_date": "20250716",
      "code_info": "All LikoScale Adapter Kits manufactured between 8/27/2013 to 2/27/2025",
      "more_code_info": ""
    }
  ]
}