{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "West Caldwell",
      "address_1": "4 Henderson Dr",
      "reason_for_recall": "Extremely low absorbance readings.",
      "address_2": "",
      "product_quantity": "731 Kits",
      "code_info": "ACE¿ ALT Reagent (Product reorder number SA1046 Lot F3604)",
      "center_classification_date": "20140429",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "NJ",
      "product_description": "Alfa Wassermann Diagnostic Technologies, LLC.  ACE ALT Reagent.      Product Usage:  For quantitative determination of ALT in serum and lithium heparin plasma using ACE¿, ACE Alera¿ and ACE Axcel\u001d Clinical Chemistry Systems. This test is intended for use in clinical laboratories and physician office labs.",
      "report_date": "20140507",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alfa Wassermann, Inc.",
      "recall_number": "Z-1529-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "67897",
      "termination_date": "20150813",
      "more_code_info": "",
      "recall_initiation_date": "20140305",
      "postal_code": "07006-6608",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}