{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "217382",
      "product_res_number": "Z-0876-2026",
      "event_date_initiated": "2025-11-13",
      "event_date_posted": "2025-12-02",
      "recall_status": "Open, Classified",
      "res_event_number": "97987",
      "product_code": "JTR",
      "product_description": "KWIK-STIK, Quality control kit for culture media, Vibrio parahaemolyticus derived from ATCC 17802, Catalog Number 0818K",
      "code_info": "UDI-DI: 30845357020018;\nLot Number: 818-111-7",
      "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": "Rebecca Neu\n320-229-7080",
      "reason_for_recall": "Some products packaged for lot 818-111-7 may have been packaged in pouches labeled as lot 857-53-10.",
      "root_cause_description": "Under Investigation by firm",
      "action": "An Urgent Medical Device Recall notification letter dated 11/13/25 was sent to customers.\n\nINSTRUCTIONS:\n1.CONTACT END USERS who have received or may have received the affected items above and provide them with the Customer Communication and Customer Response Forms.\n2.COMPLETE the Distributor Response Form provided.\n3.RETURN the response forms to recall@microbiologics.com.\n4.KEEP this letter for your records.\n5.CONTACT Microbiologics if a replacement kit is needed.\n\nMicrobiologics is dedicated to ensuring the success of your quality control processes. Please contact our Recall Support team at 320.229.7080 or recall@microbiologics.com with questions or concerns. Collect calls may be made.",
      "product_quantity": "5 units",
      "distribution_pattern": "International distribution to the countries of UAE, China, Singapore, Kazakhstan,",
      "openfda": {
        "k_number": [
          "K842129",
          "K830133",
          "K821660",
          "K820064",
          "K842579",
          "K812698",
          "K831653",
          "K855198",
          "K862914",
          "K871121",
          "K861022",
          "K822954"
        ],
        "device_name": "Kit, Quality Control For Culture Media",
        "medical_specialty_description": "Microbiology",
        "regulation_number": "866.2480",
        "device_class": "1",
        "registration_number": [
          "3006091463",
          "2518630",
          "1050138",
          "3015715780",
          "2030538",
          "1924669",
          "9610649",
          "2150138",
          "2436875"
        ],
        "fei_number": [
          "3006091463",
          "2518630",
          "1050138",
          "3015715780",
          "1000520007",
          "3002807578",
          "1000521444",
          "2150138",
          "1924669"
        ]
      }
    }
  ]
}