{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Saint Paul",
      "address_1": "3m Center 2510 Conway Ave , B# 275-5-W-6",
      "reason_for_recall": "3M discovered that the Futuro\" Quick Strap Ankle Brace (Cat. #47736EN) and ACE\" Brand Deluxe Ankle brace (Cat. #207736) do not have the correct labeling. The products contain natural latex rubber, but do not include the appropriate caution statement.",
      "address_2": "",
      "product_quantity": "162,348 units",
      "code_info": "All lots",
      "center_classification_date": "20180309",
      "distribution_pattern": "US and Australia, Jordan, Republic Of Korea, Lebanon, New Zealand, Oman, Qatar, Taiwan, United Arab Emirates",
      "state": "MN",
      "product_description": "ACE (TM) BRAND, DELUXE ANKLE BRACE, 207736, UPC  0 51131 20387 7",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "3M Company - Health Care Business",
      "recall_number": "Z-0946-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79051",
      "termination_date": "20210211",
      "more_code_info": "",
      "recall_initiation_date": "20180131",
      "postal_code": "55144-0001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}