{
  "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": "Terminated",
      "city": "Benton Harbor",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86034",
      "recalling_firm": "Whirlpool Corporation",
      "address_1": "World Headquarters",
      "address_2": "N/A",
      "postal_code": "49022",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "The products were distributed to the following US states: MI.",
      "recall_number": "Z-2815-2020",
      "product_description": "PAPR (Powered Air-Purifying Respirator) - Model# WLPAPR20W1",
      "product_quantity": "528 units",
      "reason_for_recall": "The rivets that secure the elastic headband to the face shield have the potential to be mis-assembled. When this condition occurs, it can result in a  headband that can become loose from face shield allowing the face shield to shield on the user.",
      "recall_initiation_date": "20200702",
      "center_classification_date": "20200814",
      "termination_date": "20210625",
      "report_date": "20200826",
      "code_info": "Lot code: JX20 (or week #20 of 2020)"
    }
  ]
}