{
  "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": "Nanjing",
      "state": "N/A",
      "country": "China",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "81176",
      "recalling_firm": "Micro-Tech (Nanjing) Co., Ltd.",
      "address_1": "High Tech",
      "address_2": "NO. 10 Gaoke Third Road Nanjing National",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution in the states of AL, CA, IN, FL, GA, MO, MT, NV, OK, OR, PA TX & Washington D.C.",
      "recall_number": "Z-0237-2019",
      "product_description": "Single-Use Biopsy Forceps, JUMBO ALLIGATOR,3.2mm,  REF Catalog No. NBF13-01130230, UPN BF40180 (Pouch level) - BF40181(Case box level)  BF40182 (Carton box level) - BF40183(Over shipper level), STERILE",
      "product_quantity": "1360 pcs",
      "reason_for_recall": "Single-Use Biopsy Forceps box contains incorrect product, instead it contains some Grasping Forceps units",
      "recall_initiation_date": "20180920",
      "center_classification_date": "20181023",
      "termination_date": "20191021",
      "report_date": "20181031",
      "code_info": "Lot Number - M180409031  Date of Manufacture - 20180409  Use By - 20220408"
    }
  ]
}