{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Norwood",
      "address_1": "2 Edgewater Drive",
      "reason_for_recall": "RAPIDPoint 500 Measurement Cartridges may have an error code  one or more electrolyte parameters (e.g., Na+, Ca++, K+, Cl-)",
      "address_2": "",
      "product_quantity": "20,507 cartridges",
      "code_info": "Serial Numbers:  2334500011 through 2412705915",
      "center_classification_date": "20140718",
      "distribution_pattern": "Nationwide  Foreign:  U.A.E.  Albania  Austria  Australia  Bosnia Herzeg.  Belgium  Bulgaria  Bahrain  Brazil  Canada  Switzerland  P.R. China  Colombia  Czech Republic  Germany  Denmark  Algeria  Estonia  Egypt  Spain  Finland  France  United Kingdom  Georgia  Greece  Hong Kong  Croatia  Hungary  Indonesia  Ireland  Israel  India  Italy  Japan  Republic Korea  Kuwait  Lithuania  Luxembourg  Latvia  Malaysia  Mexico  Netherlands  Norway  New Zealand  Peru  Poland  Portugal  Qatar  Romania  Serbia  Russian Fed.  Saudi Arabia  Sweden  Singapore  Slovenia  Turkey  Taiwan",
      "state": "MA",
      "product_description": "RAPIDPoint 500 Measurement Clinical Chemistry System  RAPIDPoint 500 Measurement Cartridge Lactate (750 Tests)  Part number: 10491449;  RAPIDPoint 500 Measurement Cartridge Lactate (400 Tests)  Part Number: 10491448  RAPIDPoint 500 Measurement Cartridge Lactate (250 Tests)  Part Number: 10491447  RAPIDPoint 500 Measurement Cartridge Lactate (100 Tests)  Part Number:10844813",
      "report_date": "20140730",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Siemens Healthcare Diagnostics Inc",
      "recall_number": "Z-2079-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68437",
      "termination_date": "20150610",
      "more_code_info": "",
      "recall_initiation_date": "20140523",
      "postal_code": "02062",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
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}