{
  "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": "Ongoing",
      "city": "Irvine",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86988",
      "recalling_firm": "Medtronic Neurosurgery",
      "address_1": "5290 California Ave",
      "address_2": "N/A",
      "postal_code": "92617-3073",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution.  US nationwide, Albania, Argentina, Armenia, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, Chile, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Dominican Republic, Egypt, Finland, Germany, Greece, Guam, Hong Kong, Hungary, India, Islamic Republic of Iran, Ireland, Israel, Italy, Latvia, Macao, Malaysia, Mauritius, Republic of Moldova, Netherlands, New Zealand, Nigeria, Norway, Pakistan, Poland, Portugal, Qatar, Saudi Arabia, Serbia, Singapore, South Africa, Spain, Sweden, Switzerland, Taiwan, Thailand, United Arab Emirates, United Kingdom, and Vietnam",
      "recall_number": "Z-0740-2021",
      "product_description": "Medtronic Ares Antibiotic-Impregnated Catheter, REF: 95001, Sterile, Rx Only.  Used in the treatment of hydrocephalus as a component of a shunt system when draining or shunting of cerebrospinal fluid (CSF) is indicated.",
      "product_quantity": "3,858 units",
      "reason_for_recall": "There is a potential for a defect on the seal of the outer pouch of catheters. The defect may compromise the sterility of the pouch contents, which may increase the risk of post-operative infection, requiring further medical intervention.",
      "recall_initiation_date": "20201208",
      "center_classification_date": "20201228",
      "report_date": "20210106",
      "code_info": "Lot Numbers: 0010038455,  0010258429,  0010289822,  0010316971,  0010376783,  0010061294,  0010258430,  0010289823,  0010316972,  0010384872,  0010061295,  0010258433,  0010297674,  0010316973,  0010384874,  0010083617,  0010265129,  0010297675,  0010336621,  0010384881,  0010083618,  0010265130,  0010297676,  0010336622,  0010384888,  0010083619,  0010265131,  0010297683,  0010336623,  0010393228,  0010083620,  0010265133,  0010305904,  0010353498,  EB00006085,  0010083622,  0010265134,  0010305905,  0010353499,  EB00006086,  0010083623,  0010265135,  0010305906,  0010369357,  EB00006166,  0010097240,  0010278428,  0010305907,  0010369358,  EB00007496,  0010097241,  0010278430,  0010305908,  0010369359,  EB00007537,  0010097249,  0010281382,  0010305909,  0010376779,  EB00009476,  0010097250,  0010281383,  0010316967,  0010376781,  0010097251,  0010289819,  0010316968,  0010376782"
    }
  ]
}