{
  "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": [
    {
      "status": "Terminated",
      "city": "Lenexa",
      "state": "KS",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "65476",
      "recalling_firm": "Remel Inc",
      "address_1": "12076 Santa Fe Trail Dr",
      "address_2": "N/A",
      "postal_code": "66215-3519",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide Distribution",
      "recall_number": "Z-0537-2014",
      "product_description": "Streptex* kit, Ref R30950501 ZL50, Rapid latex test for Streptococcal grouping, IVD.  The kit contains reagent groups A, B, C, D, F, G, a control, and an extraction enzyme.  The firm name on the label is Remel Europe Ltd., Dartford, England.    Streptex is a rapid latex test system for use in the qualitative detection and identification of the Lancefield group of streptococci. Reagents are provided for groups A, B, C, D, F and G covering the majority of clinical isolates, group E streptococci are rarely isolated.",
      "product_quantity": "768 kits",
      "reason_for_recall": "The product may give weak or false negative test results.",
      "recall_initiation_date": "20130502",
      "center_classification_date": "20131218",
      "termination_date": "20140312",
      "report_date": "20131225",
      "code_info": "Lot 1192181, exp. January 2014"
    }
  ]
}