{
  "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": "Santa Clara",
      "state": "CA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82011",
      "recalling_firm": "Lin-Zhi International Inc",
      "address_1": "2945 Oakmead Village Ct",
      "address_2": "N/A",
      "postal_code": "95051-0812",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide Distribution in the states of CA, MA, GA, KY, NC, MI, MD, NC, CT, AZ SC, TN, OR",
      "recall_number": "Z-1256-2019",
      "product_description": "Ethyl Alcohol Enzymatic Assay, (a) REF 0220 (small test kit), (b) REF 0221 (large test kit)    Product Usage:  Detergent causes faster degradation in EtOH assay. Possible container or pitchers with some detergent residue  was used while producing R2 of the defective lot.",
      "product_quantity": "49 kits",
      "reason_for_recall": "Shelf life of the product may be reduced due to degradation of the assay.",
      "recall_initiation_date": "20190111",
      "center_classification_date": "20190502",
      "termination_date": "20210322",
      "report_date": "20190508",
      "code_info": "(a) REF 0220 (small test kit), Lot Code 1810026  (b) REF 0221 (large test kit), Lot Code 1810025"
    }
  ]
}