{
  "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": "161054",
      "product_res_number": "Z-0622-2018",
      "event_date_initiated": "2017-12-20",
      "event_date_created": "2018-02-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-12-08",
      "res_event_number": "78997",
      "product_code": "HBO",
      "k_numbers": [
        "K050044"
      ],
      "product_description": "Model #: CG8900, Medtronic Clip Gun Scalp Clip Kit (Qty 1); Model #: CG8901, Medtronic Clip Gun Scalp Clip Kit (Qty 10); Model #: CG8901A, Medtronic Clip Gun Applicator (Qty 10)",
      "code_info": "Affected Lots: D80412, D84100, E00008, E00983, E03049, E03716, E05806, E07257, E09145, E14782, E14896, E15195, E19181, E19182, E19183, E19184, E19868, E20599, E23631, E33102, D80413, D84101, E00009, E00984, E03050, E03717, E05233, E05807, E07258, E09117, E09146, E09239, E11242, E11243, E11244, E11706, E12011, E12012, E13574, E14784, E14898, E15197, E19185, E19186, E19187, E19188, E19869, E20600, E23768, E23769, E23770, E23771, E23772, E23773, E23774, E33103, E33104, E33105, E33106, E33107, E33108, E33109, E33110, E33454, E34928, E05810, E09149, E19194, E19871, E23775, E33099",
      "firm_fei_number": "3015531529",
      "recalling_firm": "Medtronic Neurosurgery",
      "address_1": "125 Cremona Dr",
      "city": "Goleta",
      "state": "CA",
      "postal_code": "93117-3083",
      "additional_info_contact": "805-571-8400",
      "reason_for_recall": "Medtronic is initiating a voluntary recall because the products identified above did not adequately demonstrate acceptable packaging performance to current standards.",
      "root_cause_description": "Package design/selection",
      "action": "A Consignee Notification with response form was sent to affected consignees on 12/20/2017.",
      "product_quantity": "27,432.8 devices",
      "distribution_pattern": "Algeria, Armenia, Australia, Canada, Cyprus, Egypt, Germany, Ghana, Greece, Guam, Iceland, Indonesia, Iran, Italy, Jordan, New Zealand, Poland, Portugal, Puerto Rica, Russian Federation, Saudi Arabia, Singapore, South Africa, Spain, Swaziland, Sweden, Switzerland, Syria, Tunisia, Turkey, UAE, UK, USA, Yemen",
      "openfda": {
        "k_number": [
          "K944311",
          "K894778",
          "K033660",
          "K896723",
          "K012219",
          "K883963",
          "K253814",
          "K905433",
          "K050044",
          "K890443",
          "K881265"
        ],
        "registration_number": [
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        "fei_number": [
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        ],
        "device_name": "Clip, Scalp",
        "medical_specialty_description": "Neurology",
        "regulation_number": "882.4150",
        "device_class": "2"
      }
    }
  ]
}