{
  "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": "2026-09-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "214023",
      "product_res_number": "Z-2340-2025",
      "event_date_initiated": "2025-07-08",
      "event_date_posted": "2025-08-19",
      "recall_status": "Open, Classified",
      "res_event_number": "96916",
      "product_code": "NHL",
      "pma_numbers": [
        "P150031"
      ],
      "product_description": "Burr Hole Cover Kit, REF: M365DB4600C0;  Burr Hole Cover Spares Kit, REF: M365DB4605C0. Components of Vercise Deep Stimulation System used with the Surgical Implant Manual",
      "code_info": "All lots.\nSurgical Implant Manual version\nREF/UDI-DI:\nM365DB4600C0/08714729820802,\t\nM365DB4605C0/08714729820819",
      "firm_fei_number": "3006630150",
      "recalling_firm": "Boston Scientific Neuromodulation Corporation",
      "address_1": "25155 Rye Canyon Loop",
      "city": "Valencia",
      "state": "CA",
      "postal_code": "91355-5004",
      "additional_info_contact": "661-949-4000",
      "reason_for_recall": "Resistance and difficulties could occur while closing the retaining clip locking mechanism, which is part of a burr hole cover kit, which is part of a Deep Brain Stimulation (DBS) system, which may lead to procedural delay, or lead-migration-which may require additional surgery.",
      "root_cause_description": "Component change control",
      "action": "On 7/8/2025, correction notices were mailed, emailed, or delivered to healthcare professionals who were asked to do the following:\n\n1. Review the updates to the Surgical Implant Manual stated in this notice.  These updates will be found in the IFU once implemented.\n2. If you are a facility that has sent products to another hospital or a facility within\nyour network, ensure this notification is forwarded to them.\n3. If you are a distributor, this notification must be forwarded to your customers to\nensure this notification is carried out to the end-user level.\n4. To provide awareness of this information, share this letter with any other clinicians\nin your hospital who use these devices.\n5. If users encounter resistance or difficulties while closing the Retaining Clip locking\nmechanism, refer to the Surgical Implant Manual updates provided.\n6. Maintain a copy of this letter in your facility s records.\n7. Complete and return the acknowledgement form via email to BSCFieldActionCenter@bsci.com\n\nThe Surgical Implant Manual has updates that include:\n- If you have difficulty locking the Slider, you may need to remove the Lead Stylet before locking the Slider in place, or replace the Retaining Clip using another Burr Hole Cover Kit or Burr Hole Cover Spares Kit. \n- You may confirm the Slider is fully locked.\n- Verify that the DBS Lead has not moved from the desired location (e.g. by intraoperative imaging).\n\nReport all device-related incidents or quality concerns experienced with the use of these devices to firm at BSN.ComplaintCallCenter@bsci.com",
      "product_quantity": "24,583",
      "distribution_pattern": "Worldwide - US Nationwide distribution including in the states of MN, FL, CO, MD, NY, NE, PA, WI, AZ, TN, MO, TX, MI, MT, MA, WV, AL, VA, NC, CA, OR, WA, LA, OH, NJ, NH, SD, GA, CT, NV, UT, IN, ID, IL, ME, SC, DC, OK, KY, AK, HI, RI, AR, KS, NM and the countries of Algeria, Austria, Azerbaijan, Belgium, Bulgaria, Croatia, Denmark, Egypt, Finland, France, Georgia, Germany, Greece, Hungary, Iceland, Iran, Ireland, Israel, Italy, Jordan, Kazakhstan, Kuwait, Lebanon, Libya, Luxembourg, Malta, Morocco, Netherlands, Norway, Pakistan, Poland, Portugal, Romania, Russian Fed., Saudi Arabia, Serbia, Slovakia, South Africa, Spain, Sweden, Switzerland, T¿rkiye, UAE, Ukraine, United Kingdom, Canada, Japan, Argentina, Brazil, Chile, Colombia , Ecuador, Mexico, Hong Kong, China, India, Singapore, Korea, Taiwan.",
      "openfda": {
        "pma_number": [
          "P960009",
          "P150031"
        ],
        "registration_number": [
          "2135338",
          "3010052483",
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          "3005210579",
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          "2024311",
          "3038429246",
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          "3010086866",
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        ],
        "fei_number": [
          "3010052483",
          "3015200795",
          "2182207",
          "3009380063",
          "3005700659",
          "2648729",
          "3002618605",
          "3019807891",
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          "3013023969",
          "2124215",
          "3010972758",
          "2183744",
          "3000203466",
          "1928237",
          "3003120897",
          "3003477135",
          "3000209794",
          "3006630150",
          "3005210579",
          "3005160949",
          "3004593495",
          "3010531069",
          "3003335547",
          "3018094310",
          "1627487",
          "2024311",
          "3038429246",
          "2649622",
          "3010086866",
          "3006705815",
          "3004369318"
        ],
        "device_name": "Stimulator, Electrical, Implanted, For Parkinsonian Symptoms",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}