{
  "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": "Lachine",
      "state": "N/A",
      "country": "Canada",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84118",
      "recalling_firm": "AMD Medicom Inc.",
      "address_1": "1200 55e Ave",
      "address_2": "N/A",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed tot he following US states:  CA, FL, IA, IN, MD, MI, NV, NY, PA, SC, TN, TX, and WA.    The products were distributed to the following foreign countries:  Canada.",
      "recall_number": "Z-0495-2020",
      "product_description": "MEDICOM SAFEMASK PREMIER PLUS ASTM LEVEL 3 MASKS, Item Code 2042",
      "product_quantity": "112 cases (500 units/case)",
      "reason_for_recall": "Due to an error on the packaging line, some level 2 masks may have been packed in some level 3 mask boxes. The two masks are visually indistinguishable, causing the risk of using a mask with a lower protection level than intended.",
      "recall_initiation_date": "20191011",
      "center_classification_date": "20191119",
      "termination_date": "20210914",
      "report_date": "20191127",
      "code_info": "Lot 1917"
    }
  ]
}