{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "184809",
      "product_res_number": "Z-0612-2021",
      "event_date_initiated": "2020-11-19",
      "event_date_created": "2020-12-16",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-04-03",
      "res_event_number": "86907",
      "product_code": "MHY",
      "product_description": "Percept PC Implantable Neurostimulator (INS) - Product Usage: The Percept PC is a neurostimulation device for deep brain stimulation therapy. It is indicated for DBS treatment for Parkinson s disease, essential tremor, dystonia, obsessive-compulsive disorder, and epilepsy.",
      "code_info": "Model Number: B35200; GTIN: 00763000253363; Serial Numbers: NPI706941H, NPI707024H, NPI707000H, NPI706992H, NPI706963H, NPI706962H, NPI706987H, NPI706945H, NPI706952H, NPI706954H, NPI706955H, NPI706957H",
      "firm_fei_number": "2182207",
      "recalling_firm": "Medtronic Neuromodulation",
      "address_1": "7000 Central Ave Ne",
      "city": "Minneapolis",
      "state": "MN",
      "postal_code": "55432-3568",
      "additional_info_contact": "David Young\n800-707-0933",
      "reason_for_recall": "A software anomaly in the A620 Patient Programmer application was identified that results in failure to connect with the Percept PC device.",
      "root_cause_description": "Software design",
      "action": "Beginning November 19, 2020 accounts impacted by this issue were verbally notified to quarantine affected product. \nBeginning November 25, 2020 a recall notification letter and retrieval instructions titled \"URGENT: MEDICAL DEVICE RECALL A620 Patient Programmer issue with specific Percept\" PC Neurostimulators\" was hand delivered to impacted accounts by Medtronic Representatives.",
      "product_quantity": "12 devices",
      "distribution_pattern": "US Nationwide distribution including in the states of Arizona, California, New Hampshire, Pennsylvania, Tennessee, Texas, Washington.",
      "openfda": {
        "pma_number": [
          "P960009",
          "P140009"
        ],
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        ],
        "device_name": "Stimulator, Electrical, Implanted, For Parkinsonian Tremor",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}