{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
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  "results": [
    {
      "country": "United States",
      "city": "Plano",
      "address_1": "6901 Preston Rd",
      "reason_for_recall": "The firm received complaints of error messages that occurred during routine impedance checks on Proclaim DRG IPGs, model 3664.  Some complaints were also associated with transient over stimulation which created discomfort for the patients.",
      "address_2": "",
      "product_quantity": "17 units",
      "code_info": "Lot Number 6210849  Serial Number AVM174.1    Lot Number 6210852  Serial Numbers:  AVA560.1, AVA214.1, AVL027.1    Lot Number 6499208  Serial Numbers:  AVD426.1, AVA922.1    Lot Number 6263128  Serial Numbers:  AVB119.1, AVD400.1, AVA622.1, AVD431.1, AVE633.1,   AVK678.1, AVN837.1     Lot Number 6268723  Serial Numbers:   AUV770.1, AVW805.1    Lot Number 6278155  Serial Number AVK896.1",
      "center_classification_date": "20180323",
      "distribution_pattern": "US",
      "state": "TX",
      "product_description": "Proclaim DRG Implantable Pulse Generator, Model Number 3664",
      "report_date": "20180404",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "St. Jude Medical, Inc.",
      "recall_number": "Z-1170-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79560",
      "termination_date": "20201103",
      "more_code_info": "",
      "recall_initiation_date": "20180309",
      "postal_code": "75024-2508",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}