{
  "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": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87954",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "N/A",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the states of OH, CO, CA, IL, FL, VA, TX, MN, GA, WA, MA, MD, NY, LA, AZ, OR.",
      "recall_number": "Z-1948-2021",
      "product_description": "Medical Action INDUSTRIES INC., General Purpose Instrument Tray, REF 61209",
      "product_quantity": "102 cases of 20 units",
      "reason_for_recall": "There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits",
      "recall_initiation_date": "20210511",
      "center_classification_date": "20210624",
      "termination_date": "20230510",
      "report_date": "20210630",
      "code_info": "Batch Numbers:  0000277610, Exp. 04/15/2022; 0000276879, Exp. 04/15/2022"
    }
  ]
}