{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "cfres_id": "42908",
      "product_res_number": "Z-0202-06",
      "event_date_initiated": "2003-03-28",
      "event_date_posted": "2005-11-26",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-10-29",
      "res_event_number": "34010",
      "product_code": "FPO",
      "k_numbers": [
        "K862441"
      ],
      "product_description": "PROFlex Transporter, Model number 35P. The catalog number for the model 35P is PT3550.",
      "code_info": "All stretchers containing a serial number beginning with the letter ''L'' and followed by a sequence of six numbers.",
      "firm_fei_number": "1523574",
      "recalling_firm": "Ferno-Washington Inc",
      "address_1": "70 Weil Way",
      "city": "Wilmington",
      "state": "OH",
      "postal_code": "45177-9371",
      "additional_info_contact": "Dorothy Deaton\n937-382-1451",
      "reason_for_recall": "The firm received complaints of the stretchers folding. A fold is when the stretcher lowers on its own to either the next position, or any of the other seven postions of the stretcher.",
      "root_cause_description": "Other",
      "action": "The firm went out to customers who had complained of a 'fold' and installed the kit on the stretcher that had experienced the fold and on all other PROflexx stretchers owned by the customer. These customers had received a recall letter, dated March 28, 2003. For customers that had not complained of the stretchers 'folding', the firm sent a letter dated June 24, 2003, to all distributors requesting the distributor provide the firm with a list of customers that had received the PROflex stretchers. Once the firm had a list of all customers, they sent them a letter offering them the kit as an enhancement that they could purchase to help reduce the possibility of false locking.",
      "product_quantity": "2188 total stretchers",
      "distribution_pattern": "The product was distributed nationwide to 27 states: TN, MA, VT, IL, KY, NY, SC, WI, TX, MO, NH, CO, GA, NC, CA, VA, IA, PA, CT, OH, NJ, ID, WV, AL, AR, ME and IN.",
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        "device_name": "Stretcher, Wheeled",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6910",
        "device_class": "2"
      }
    }
  ]
}