{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "34668",
      "product_res_number": "Z-0570-05",
      "event_date_initiated": "2004-08-18",
      "event_date_posted": "2005-03-08",
      "recall_status": "Terminated",
      "event_date_terminated": "2012-04-12",
      "res_event_number": "29856",
      "product_code": "LZH",
      "k_numbers": [
        "K944669"
      ],
      "product_description": "Flexiflo Quantum Enteral Pump",
      "code_info": "Serial #1061305 through 1061455 Serial #1061486 through 1061505 Serial #1061507 through 1061512 Serial #1061705 through 1061726",
      "firm_fei_number": "1000136098",
      "recalling_firm": "Ross Products Division Abbott Laboratories",
      "address_1": "625 Cleveland Ave",
      "city": "Columbus",
      "state": "OH",
      "postal_code": "43215-1754",
      "additional_info_contact": "Randal P. McCay\n614-624-7677",
      "reason_for_recall": "Pumps were manufactured with  an incorrect circuit board that may cause an increase in the feed rate and flush frequency of fluids.",
      "root_cause_description": "Other",
      "action": "The firm contacted all consignees via telephone and letter on 08/18/2004.",
      "product_quantity": "199 individual serial numbered units",
      "distribution_pattern": "Products were distributed to the following states nationwide: MA, NJ, NY, PA, MD, VA, NC, SC, GA, FL, CA, TN, KY, OH, MI, SD, IL, KS, LA, AR, OK, TX, and CO.",
      "openfda": {
        "k_number": [
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          "K040957",
          "K913958",
          "K914216",
          "K200051",
          "K946168",
          "K945964",
          "K060316",
          "K221603",
          "K981541",
          "K031407",
          "K232205",
          "K011587",
          "K873119",
          "K923066",
          "K143263",
          "K011868",
          "K111381",
          "K901458",
          "K220230",
          "K040196",
          "K940555",
          "K913413",
          "K954735",
          "K253558",
          "K003047",
          "K951429",
          "K141479",
          "K153074",
          "K031199",
          "K940556",
          "K891575",
          "K943733",
          "K952671"
        ],
        "device_name": "Pump, Infusion, Enteral",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2",
        "registration_number": [
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    }
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}