{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "131512",
      "product_res_number": "Z-0578-2015",
      "event_date_initiated": "2014-11-13",
      "event_date_posted": "2014-12-12",
      "recall_status": "Terminated",
      "event_date_terminated": "2015-01-29",
      "res_event_number": "69771",
      "product_code": "JSK",
      "k_numbers": [
        "K831469"
      ],
      "product_description": "Oxoid Legionella BCYE Growth Supplement packaged in packs of 10-100ml vials.  \n\nA growth supplement for the isolation of Legionella.",
      "code_info": "Lot number: 1374439, Exp: 31 Aug 2015",
      "firm_fei_number": "1924669",
      "recalling_firm": "Remel Inc",
      "address_1": "12076 Santa Fe Trail Dr",
      "city": "Lenexa",
      "state": "KS",
      "postal_code": "66215-3519",
      "additional_info_contact": "Scott A. Kendall\n770-409-0713",
      "reason_for_recall": "Use of the product could result in inadequate recovery of Legionella pneumophila which could result in false negative reporting.",
      "root_cause_description": "Under Investigation by firm",
      "action": "ThermoFisher sent an Urgent Medical Device Recall letter dated November 13, 2014, to the sole customer.  The letter identified the product, the problem, and the action to be taken by the customer.  Customers were instructed to notify any personnel who need to be aware of the potential for false negative identification of the affected product.  Review their inventory for the affected product and discard it.  Customers were also instructed to completed the attached Medical Device Recall Return Response acknowledging receipt of the notice and disposal of the affected product.  If further distributed customers should contact those entities, advise them of the situation and provide them with a copy of the letter.  Customers with questions were instructed to contact their Technical Services Department at 800-255-6730.",
      "product_quantity": "1/10/100 ml/vials/packs",
      "distribution_pattern": "Nationwide Distribution to FL",
      "openfda": {
        "k_number": [
          "K800258",
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          "K810591",
          "K800265",
          "K811653",
          "K861823",
          "K800260",
          "K850299",
          "K800266"
        ],
        "device_name": "Supplement, Culture Media",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.2450",
        "device_class": "1",
        "registration_number": [
          "3006091463",
          "3005182159",
          "3015715780",
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}