{
  "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": "Union City",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85533",
      "recalling_firm": "Abaxis Inc",
      "address_1": "3240 Whipple Rd",
      "address_2": "",
      "postal_code": "94587-1217",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "All U.S. Consignees, TX, PA, FL, OK, KY, CA, VA  No OUS Consignees.",
      "recall_number": "Z-2361-2020",
      "product_description": "Piccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II)",
      "product_quantity": "15",
      "reason_for_recall": "Incorrect reference ranges of analytes.",
      "recall_initiation_date": "20191211",
      "center_classification_date": "20200612",
      "termination_date": "20220722",
      "report_date": "20200624",
      "code_info": "Model Number: 1100-0000; 1100-0001; Software version 2.1.55 (NGA models )/3.1.35(Jen II models)  Serial Numbers:0000000P23019,  0000000P02700  0000000P22997,   0000000P24435  0000000P05910  0000000P05380  0000000P08467  0000000P06595  0000000P07622  0000000P07988  0000000P04609  0000000P24721  0000000P24495  0000000P20399  0000000P20131  0000000P02755",
      "more_code_info": ""
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}