{
  "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": "78444",
      "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": "AL, AR, AZ, CA, CO, CT, DE, FL, GA, IA, IL, IN,  KS, KY, LA, MD, MI, MO, MS, NC, NH, NY, OH,  OR, PA, SC, TN, TX, UT, VA, WI, WV",
      "recall_number": "Z-0552-2018",
      "product_description": "ACE(TM) BRAND, ULTRA LITE ANKLE brace: (a) Size Selection Medium, Cat #901014, UPC 051131019984 2; (b) Size Selection Large, Cat #901015, UPC 0 51131019985 9",
      "product_quantity": "996 units",
      "reason_for_recall": "Mold was found on the non-patient contact  surfaces of the product and was identified as  Aspergillus candidus.",
      "recall_initiation_date": "20171101",
      "center_classification_date": "20180207",
      "termination_date": "20200722",
      "report_date": "20180214",
      "code_info": "(a) Cat #901014, Lot Numbers:  7223T2, 7133C2, 7144E2,  7332I2  (b) Cat #901015, Lot Number 7223U2"
    }
  ]
}