{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Portage",
      "state": "MI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79779",
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "address_1": "4100 E Milham Ave",
      "address_2": "N/A",
      "postal_code": "49002-9704",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide and Ireland, Japan, South Korea, UK",
      "recall_number": "Z-1510-2018",
      "product_description": "T5 Zipper Toga with Peel-Away Face Shield, (XL/T); Catalog number: 0400-850-100  Sterile personal protection garment",
      "product_quantity": "34570 total products",
      "reason_for_recall": "Separation of material layers may occur, causing a potential risk of exposure to contaminants.",
      "recall_initiation_date": "20180223",
      "center_classification_date": "20180424",
      "termination_date": "20190523",
      "report_date": "20180502",
      "code_info": "Lot numbers: 17061837, 17061859, 17113164"
    }
  ]
}