{
  "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": "Completed",
      "city": "Mounds View",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "89054",
      "recalling_firm": "Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)",
      "address_1": "8200 Coral Sea St Ne",
      "address_2": "",
      "postal_code": "55112-4391",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US, Canada, Northern Mariana Islands",
      "recall_number": "Z-0391-2022",
      "product_description": "Medical Device Identification Cards associated with Astra XT DR Implantable pulse generator",
      "product_quantity": "10 Medical Device Cards",
      "reason_for_recall": "The back of some Medical Device Identification Cards provided to patients were printed with an erroneous statement stating the following:  \"This patient has a complete MR conditional system implanted.\"",
      "recall_initiation_date": "20211108",
      "center_classification_date": "20211216",
      "report_date": "20211222",
      "code_info": "Astra XT DR implantable pulse generator, Product Number/CFN X2DR01,   UDI 00763000108953, Serial Numbers:   RNH655287S, RNH648107S, RNH645452S, RNH634608S, RNH642593S, RNH638740S, RNH635040S, RNH636809S, RNH633755S    UDI 00643169634671, Serial Numbers:  RNH612514S",
      "more_code_info": ""
    }
  ]
}