{
  "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
    }
  },
  "results": [
    {
      "cfres_id": "191717",
      "product_res_number": "Z-0641-2022",
      "event_date_initiated": "2013-03-25",
      "event_date_created": "2022-02-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2022-04-22",
      "res_event_number": "89479",
      "product_code": "JTR",
      "k_numbers": [
        "K861022"
      ],
      "product_description": "KWIK-STIK(TM), Quality control kit for culture media, sold as: \n\nKWIK-STIK(TM) 2-pack Enterococcus faecalis derived from ATCC(R) 51299(TM)",
      "code_info": "Catalog Number 01023P, UDI: 20845357029502, Lot Number (Expiration Date): 1023-05-7 (04/30/2014)",
      "firm_fei_number": "2150138",
      "recalling_firm": "Microbiologics Inc",
      "address_1": "200 Cooper Ave N",
      "city": "Saint Cloud",
      "state": "MN",
      "postal_code": "56303-4440",
      "additional_info_contact": "Becky Neu\n320-229-7073",
      "reason_for_recall": "Some of the KWIK-STIK Catalog #01023P Campylobacter coli, Lot# 1023-05-7, contained an inner label stating the product is Catalog #0919K Haemophilus influenza. The organism has been confirmed to be C. coli, indicating this is a labeling error and the organism is the correct organism.",
      "root_cause_description": "Labeling mix-ups",
      "action": "Microbiologics notified customers on 03/25/2013 via letter titled \"Important Medical Device Correction\". Instructions included to inspect inventory for affected products. If customers have received the product identified within the recall (KWIK-STIK\" 01023P, Lot# 1023-05-7), it is recommended that the customer destroys the product. Microbiologics shall replace the destroyed product upon confirmation of destruction.\n\nQuestions or concerns can be directed to the Customer Service Manager at 320.229.7057.",
      "product_quantity": "10 units",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada, South Africa, France, Netherlands, Mauritius, China.",
      "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"
        ],
        "fei_number": [
          "1000521444",
          "2518630",
          "2150138",
          "3002807578",
          "1050138",
          "1924669",
          "3006091463",
          "1000520007",
          "3015715780"
        ]
      }
    }
  ]
}