{
  "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": [
    {
      "country": "United States",
      "city": "Saint Paul",
      "address_1": "4100 Hamline Ave N Bldg 3",
      "reason_for_recall": "There is a potential for the Pacing System Analyzer (PSA) to exhibit unintended cross-chamber stimulation.",
      "address_2": "",
      "product_quantity": "74 units",
      "code_info": "Serial Numbers:  001343  000488  000903  001404  000923  001352  001441  000203  000224  000255  000284  000434  000441  000445  000501  000515  000519  000521  000534  000536  000546  000553  000578  000588  000601  000602  000605  000606  000609  000610  000616  000617  000620  000628  000631  000633  000634  000636  000637  000638  000643  000644  000661  000664  000666  000667  000669  000671  000673  000677  000679  000682  000688  000690  000691  000700  000710  000717  000719  000720  000723  000726  000746  000757  000765  000924  001125  001556  001562  001564  001571  001574  001615  000598",
      "center_classification_date": "20180927",
      "distribution_pattern": "Worldwide distribution - US Nationwide in the State of  FL, UT,  and VA, and countries of  Austria, Czech Republic, Germany, Greece, Netherlands, Norway, Portugal, Spain, Sweden, United Kingdom, Switzerland",
      "state": "MN",
      "product_description": "Model 3300 LATITUDE(TM) Programming System     Product Usage - The Boston Scientific LATITUDE Programming System is intended for use in hospital and clinical environments to communicate with Boston Scientific implantable systems. The software in use controls all communication functions for the Pulse Generator (PG). Detailed software applications instructions can be found in the associated product literature for the PG being interrogated.",
      "report_date": "20181003",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Boston Scientific Corporation",
      "recall_number": "Z-3260-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "81006",
      "termination_date": "20210922",
      "more_code_info": "",
      "recall_initiation_date": "20180910",
      "postal_code": "55112-5700",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}