{
  "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": "Completed",
      "city": "Lawrenceville",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71130",
      "recalling_firm": "Stradis Healthcare, LLC.",
      "address_1": "805 Marathon Pkwy Ste 100",
      "address_2": "N/A",
      "postal_code": "30046-2885",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US nationwide to AL, AK, CA, DE, FL, GA, HI, ID, IL, IN, KS, KY, ME, MD, MA, MI, MS, MO, NM, NJ, NY, NC, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA; Canada and Dubai",
      "recall_number": "Z-2019-2015",
      "product_description": "Abdominal Pack and Abdom Pack - contains Devon Light Glove  Used during surgery",
      "product_quantity": "2",
      "reason_for_recall": "Convenience kits being recalled due to the recall by the manufacturer (Medtronic) of a component (Devon Light Glove) contained in the kits.",
      "recall_initiation_date": "20150420",
      "center_classification_date": "20150707",
      "report_date": "20150715",
      "code_info": "Pack 670-056, 681-014"
    }
  ]
}