{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
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  },
  "results": [
    {
      "cfres_id": "65471",
      "product_res_number": "Z-0456-2008",
      "event_date_initiated": "2007-10-12",
      "event_date_posted": "2007-12-29",
      "recall_status": "Terminated",
      "event_date_terminated": "2008-06-26",
      "res_event_number": "45442",
      "product_code": "JTR",
      "k_numbers": [
        "K861022"
      ],
      "product_description": "MicroBiologics;  P. vulgaris, DuoPacksl Product Catalog Number: 0691P;  ARCC 0427; Exp 2008-9; MicroBiologics, St. Cloud, MN 56303.\n\n(Proteus vulgaris, Kwik-Stick,  Cat. No. 0691P)",
      "code_info": "Lot Number: 691295",
      "firm_fei_number": "2150138",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "217 Osseo Ave N",
      "city": "Saint Cloud",
      "state": "MN",
      "postal_code": "56303-4452",
      "additional_info_contact": "320-253-1640",
      "reason_for_recall": "Mislabeled: DuoPacks of Proteus vulgaris contained Listeria monocytogenes instead of the labeled Proteus vulgaris.",
      "root_cause_description": "Employee error",
      "action": "Consignees were initially notified of this recall by a telephone survey.  An Urgent Product Recall letter was sent on 10/17/07 explaining the risk to patients. The firm sent replacements of the recalled product on 10/17/07 or 10/18/07, with request for acknowledgement of Recall Notification, and certification of disposal of incorrect product.",
      "product_quantity": "20",
      "distribution_pattern": "Worldwide Distribution - USA including states of OR, PA, NY, RI, GA, SC, IL, PR, CA, AZ, and NJ, and countries of Japan, France, Colombia, and Brazil.",
      "openfda": {
        "k_number": [
          "K842579",
          "K821660",
          "K855198",
          "K820064",
          "K842129",
          "K862914",
          "K812698",
          "K861022",
          "K831653",
          "K822954",
          "K830133",
          "K871121"
        ],
        "device_name": "Kit, Quality Control For Culture Media",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.2480",
        "device_class": "1",
        "registration_number": [
          "2518630",
          "2150138",
          "1050138",
          "2436875",
          "1924669",
          "3006091463",
          "2030538",
          "9610649",
          "3015715780"
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}