{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "64647",
      "product_res_number": "Z-0145-2008",
      "event_date_initiated": "2007-05-02",
      "event_date_posted": "2007-12-19",
      "recall_status": "Terminated",
      "event_date_terminated": "2010-05-03",
      "res_event_number": "44958",
      "product_code": "MDK",
      "k_numbers": [
        "K974572"
      ],
      "product_description": "Accuprobe Group B Streptococcus Culture Identification Test, Catalog Number 2820B, Batch Number 531379, Gen-Probe, Incorporated, San Diego, CA. 92121",
      "code_info": "Catalog Number 2820B; Lot Number 531379",
      "firm_fei_number": "2024800",
      "recalling_firm": "Gen-Probe Inc",
      "address_1": "10210 Genetic Center Dr",
      "city": "San Diego",
      "state": "CA",
      "postal_code": "92121-4362",
      "additional_info_contact": "Kristin Godfredsen\n858-410-8532",
      "reason_for_recall": "Mispackaging: Kits may contain Haemophilus Influenza probe pouches in addition to Group B Streptococcus probe pouches",
      "root_cause_description": "Other",
      "action": "Gen-Probe notified customers by phone on May 2nd and 3rd, 2007; a recall notice letter was faxed to each customer on May 3rd, 2007 and mailed on May 4th, 2007 via certified mail. The letter describes the packaging error and the remote health hazard risk, and provides instructions for users to return all kits of this lot number.",
      "product_quantity": "106 kits",
      "distribution_pattern": "Nationwide: including states of AZ, CA, CO, FL, KY, MD, MO, NC, NJ, TX, and  UT",
      "openfda": {
        "k_number": [
          "K924715",
          "K915852",
          "K974572",
          "K904268"
        ],
        "device_name": "Dna-Probe, Reagents, Streptococcal",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.3740",
        "device_class": "1"
      }
    }
  ]
}