{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Indianola",
      "address_1": "1 Medrad Dr",
      "reason_for_recall": "Bayer HealthCare is recalling all MEDRAD(R) Continuum MF Infusion System tubing sets (macrobore and microbore), catalog numbers MIK200A, MIL 200B, 3015153, 3015155, 3015156, 3015157, 3015158, 3015159, and 3015161.  The firm is initiating this recall because this tubing exhibits a variation that, when used in conjunction with any Continuum pump, may result in flow rate accuracy performance issues.",
      "address_2": "",
      "product_quantity": "1,229 Pumps total",
      "code_info": "Catalog number - Primary VSA Set:  3015157.     See firm's website - www.medrad.com for specific serial and lot numbers.",
      "center_classification_date": "20121220",
      "distribution_pattern": "Worldwide distribution: USA (nationwide) and countries of: Australia, Bermuda, Brazil, Canada, China, Chile, Denmark, Dominican Republic, Estonia,  Finland, France, Germany, Great Britain, Guam, Hong Kong, India, Israel, Italy, Japan, Korea, Lebanon, Mexico, Malaysia, Netherland, Poland, Portugal, Puerto Rico, Sweden, Singapore, Taiwan, Thailand, and Venezula.",
      "state": "PA",
      "product_description": "Medrad(R) Continuum MR Infusion System Primary VSA Set    Peristaltic Pump System designed for patients who require medications and other fluids during an MR procedure. It is intended to provide infusion therapy directly prior to, during and immediately after the MR procedure functioning while either stationary or mobile.",
      "report_date": "20121226",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Medrad Inc",
      "recall_number": "Z-0600-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "61734",
      "termination_date": "20150817",
      "more_code_info": "",
      "recall_initiation_date": "20120418",
      "postal_code": "15051-9759",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}