{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Golden",
      "state": "CO",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85650",
      "recalling_firm": "CME America, LLC",
      "address_1": "14998 W 6th Ave Ste 830",
      "address_2": "N/A",
      "postal_code": "80401-5025",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S: CA, IN, LA, MO, FL, IL, ME, MN, CO, VA, OK, NE, GA, AL, KY, IA, MS, ID, TX, SC, OH, SD, NV, MI, WY, NC, PA, TN, KS, NJ, OR, AR, NM, MA, NY, DC, RI, MD, WA, WI, AZ, NH, UT, HI, AK, MT, ND, VT, CT.    OUS (Foreign): Canada, UK",
      "recall_number": "Z-2584-2020",
      "product_description": "BodyGuard Microset w/ 0.2 mic filter and lower y-site with female luer, REF: A120-160XYBF",
      "product_quantity": "6016",
      "reason_for_recall": "Infusion administration sets may have a delivery inaccuracy over plus/minus 13%, ranging from minus 42.8% to plus 17.5%. Use of the infusion pump system could cause over-infusion or under-infusion of therapy",
      "recall_initiation_date": "20200616",
      "center_classification_date": "20200715",
      "termination_date": "20220509",
      "report_date": "20200722",
      "code_info": "All lots within expiry"
    }
  ]
}