{
  "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": "2026-09-17",
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      "event_date_initiated": "2025-07-30",
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      "recall_status": "Open, Classified",
      "res_event_number": "97315",
      "product_code": "GTY",
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      "product_description": "Clearview Strep A Exact II Dipstick Respiratory Kit, CLIA Waived. Catalog Number: 4581225020",
      "code_info": "Catalog Number: 4581225020. GTIN: 10815845020024. All lot numbers",
      "firm_fei_number": "3004386693",
      "recalling_firm": "Mckesson Medical-Surgical Inc. Corporate Office",
      "address_1": "9954 Maryland Drive Deep Run Iii",
      "address_2": "Ste. 4000",
      "city": "Richmond",
      "state": "VA",
      "postal_code": "23233",
      "additional_info_contact": "Alexia Allina\n984-292-4539",
      "reason_for_recall": "Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.",
      "root_cause_description": "Process control",
      "action": "McKesson notified consignees on about 07/30/2025 via overnight mail. Consignees were instructed to immediately examine inventory and quarantine all affected units, complete and return the provided response form, and destroy any affected products. If affected product was further distributed, consignees were instructed to notify their customers.",
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      "distribution_pattern": "US Nationwide distribution in the state of Georgia.",
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        "medical_specialty_description": "Microbiology",
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