{
  "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": "2026-09-03",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "event_date_initiated": "2002-11-14",
      "event_date_created": "2002-12-02",
      "city": "Fridley",
      "address_1": "7000 Central Ave N.E.",
      "reason_for_recall": "Extended charge times prior to defibrillation shock.",
      "address_2": "Medtronic, Inc/Rice Creek Facil",
      "openfda": {},
      "product_res_number": "Z-0308-03",
      "code_info": "All serial numbers beginning with PIM4. The serial number have the form of PIM4xxxxxx.",
      "product_quantity": "2539 devices",
      "recall_status": "Open, Classified",
      "res_event_number": "25041",
      "action": "An 'Important Patient Management Information' letter, dated November 14, 2002, was sent to physicians following patients who had the defibrillators implanted and this gave recommendations to physicians to prevent the problem.",
      "distribution_pattern": "The devices have been distributed nationwide in the United States and worldwide.  2,151 units have been distributed in the United States, and 387 units have been distributed worldwide outside the U.S.",
      "product_description": "GEM DR Model 7271 Implantable Cardioverter-Defibrillator (ICD)",
      "postal_code": "55432"
    }
  ]
}