{
  "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": [
    {
      "status": "Ongoing",
      "city": "Westlake",
      "state": "OH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88877",
      "recalling_firm": "Western/Scott Fetzer Company",
      "address_1": "875 Bassett Rd",
      "address_2": "",
      "postal_code": "44145-1142",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "CT, MD, MT, OH",
      "recall_number": "Z-0268-2022",
      "product_description": "Western Oxytote DTE Digital VIPR (head only)    Model: MNDR-600",
      "product_quantity": "4974 units",
      "reason_for_recall": "VIPR (Valve Integrated Pressure Regulator) - battery rupture, causing the plastic VIPR shroud to break apart with emission of fumes and smoke",
      "recall_initiation_date": "20211016",
      "center_classification_date": "20211119",
      "report_date": "20211201",
      "code_info": "Units distributed from 05/29/20 to 08/31/21.  Digital VIPR units manufactured and distributed after 08/31/21 are outside the scope of this recall and will be recognized by a green and silver control knob sticker (green logo, silver background)",
      "more_code_info": ""
    }
  ]
}