{
  "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,
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  },
  "results": [
    {
      "cfres_id": "203580",
      "product_res_number": "Z-0212-2024",
      "event_date_initiated": "2023-10-04",
      "event_date_posted": "2023-11-02",
      "recall_status": "Open, Classified",
      "res_event_number": "93161",
      "product_code": "IOQ",
      "k_numbers": [
        "K122473"
      ],
      "product_description": "HILLROM PROGRESSA+ BED, Product Codes:  P7501A000016, P7501A000019, P7501A000031, P7501A000032, P7501A000033, P7501A000052, P7501A000053, P7501A000054, P7501A000055, P7501A001851, P7501A001972, P7501A001973, and P7501A001974",
      "code_info": "UDI/DI 00887761966925, all serial numbers",
      "firm_fei_number": "1417572",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "city": "Deerfield",
      "state": "IL",
      "postal_code": "60015-4625",
      "additional_info_contact": "Center for One Baxter\n800-422-9837",
      "reason_for_recall": "Progressa+ beds have the potential for static buildup from the casters and/or power drive. This static electricity could be passed to the operator through the transport handle during transport, resulting in a mild static electric shock.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Baxter issued an Urgent Medical Device Correction notice to its consignees on 10/04/2023 by USPS first class mail.  The notice explained the potential problem and hazard.  Baxter will be correcting this issue by installing a conductive drag chain on the Progressa+ bed frame to prevent the electrostatic charge buildup. A Baxter representative will contact your facility to schedule a device correction to add the conductive drag chain. Please note you will be receiving this correction from Baxter at no charge. All units purchased in the future will have the drag chain.",
      "product_quantity": "499 beds",
      "distribution_pattern": "US Nationwide Distribution in the states of:  CA, FL, IN, MA, NY, OH, TX, VA",
      "openfda": {
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          "K964873",
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          "K840882",
          "K882229",
          "K922140",
          "K882607",
          "K926456",
          "K912855",
          "K903659"
        ],
        "registration_number": [
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          "3031218453",
          "2030595",
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          "3003542872",
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        "fei_number": [
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          "3004411059",
          "1000518730",
          "3000204953",
          "1831750",
          "3017486514",
          "3000040879"
        ],
        "device_name": "Bed, Flotation Therapy, Powered",
        "medical_specialty_description": "Physical Medicine",
        "regulation_number": "890.5170",
        "device_class": "2"
      }
    }
  ]
}