{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25313",
      "product_res_number": "Z-0345-03",
      "event_date_initiated": "2002-11-18",
      "event_date_posted": "2002-12-18",
      "recall_status": "Terminated",
      "event_date_terminated": "2003-05-01",
      "res_event_number": "25158",
      "product_code": "JTY",
      "product_description": "Chocolate II Agar (GC II Agar with Hemoglobin and IsoVitalex), microbiological media plates.\nCatalog # 221267",
      "code_info": "Lots: 2213201 EXP 11/25/02 2213211 EXP 11/26/02 2261524 EXP 1/14/02 2246310 EXP 1/1/03 2261552 EXP 1/15/03 2276445 EXP 1/29/03",
      "firm_fei_number": "1119779",
      "recalling_firm": "Becton Dickinson & Co.",
      "address_1": "7 Loveton Circle",
      "city": "Sparks",
      "state": "MD",
      "postal_code": "21152",
      "additional_info_contact": "Becton Dickinson Regulatory Compliance\n410-316-4258",
      "reason_for_recall": "Microbiological media may exhibit No Growth or reduced colony size of Haemophilus species.",
      "root_cause_description": "Other",
      "action": "Becton Dickinson notified distributors by fax on 11/18/02 to discard inventory. Firm additionally notified distributors on 11/21/02 to include three additional lots of agar for recall. End users were notified by letter 11/21/02 to discard inventory for replacement, and return reply form.",
      "product_quantity": "6422 cartons/ 100 plates per carton",
      "distribution_pattern": "Product was sold to distributors and subsequently distributed to medical facility end users nationwide and internationally.",
      "openfda": {
        "k_number": [
          "K931864",
          "K811382",
          "K800333",
          "K770875",
          "K771035",
          "K770925",
          "K812078",
          "K771871",
          "K934331",
          "K811476",
          "K864803",
          "K822552",
          "K993033",
          "K821602",
          "K823309",
          "K881552",
          "K832948",
          "K833862",
          "K760691",
          "K840067",
          "K790368",
          "K954986",
          "K780022",
          "K821551",
          "K840159",
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          "K840065",
          "K811282",
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          "K830062",
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          "K760690",
          "K864078",
          "K841833",
          "K831124",
          "K760692",
          "K770287",
          "K791557",
          "K791554",
          "K841750",
          "K851587",
          "K800977",
          "K850841",
          "K830061",
          "K831268",
          "K881527",
          "K950196",
          "K770874",
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          "K760693",
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          "K771870",
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          "K770876",
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          "K864253",
          "K791446",
          "K771872",
          "K860384",
          "K853237",
          "K832862"
        ],
        "device_name": "Culture Media, For Isolation Of Pathogenic Neisseria",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.2410",
        "device_class": "2",
        "registration_number": [
          "1111096",
          "1924669",
          "2951280",
          "1119779",
          "2022807",
          "3009547954"
        ],
        "fei_number": [
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          "1924669",
          "1000221318",
          "1119779",
          "2022807",
          "3009547954"
        ]
      }
    }
  ]
}