{
  "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": "SA1047 lot F3609: 146; RX1047 lot F3610: 53",
      "code_info": "ACE¿ AST Reagent Product reorder numbers SA1047 (Lot F3609) and RX1047 (Lot F3610)",
      "center_classification_date": "20140429",
      "distribution_pattern": "US Nationwide Distribution",
      "state": "NJ",
      "product_description": "Alfa Wassermann Diagnostic Technologies, LLC.  ACE AST Reagent.      Product Usage:  For quantitative determination of AST 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 laboratories.",
      "report_date": "20140507",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alfa Wassermann, Inc.",
      "recall_number": "Z-1530-2014",
      "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"
    }
  ]
}