{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Saint Paul",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72780",
      "recalling_firm": "3M Company - Health Care Business",
      "address_1": "3m Center 2510 Conway Ave , B# 275-5-W-6",
      "address_2": "N/A",
      "postal_code": "55144-0001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US nationwide distribution.",
      "recall_number": "Z-0601-2016",
      "product_description": "3M Coban Self-Adherent Wrap Shipper carton label identified the product as 3M Coban LF Latex Free Catalog #2081, lot number 2018-10AM.",
      "product_quantity": "167 cases (30 rolls/case)",
      "reason_for_recall": "Product mislabeled as latex free.  Actual Catalog number 1581, lot 2020-10AN. contains latex. This could pose a health risk to  users with sensitivity or allergic reaction to latex, which could range from mild to severe.",
      "recall_initiation_date": "20151201",
      "center_classification_date": "20160106",
      "termination_date": "20160524",
      "report_date": "20160113",
      "code_info": "Catalog# 1581, lot # 2020-10AN  Catalog# 2081, lot # 2018-AM (shipper carton)"
    }
  ]
}