{
  "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": "2026-08-13",
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      "cfres_id": "42414",
      "product_res_number": "Z-0114-06",
      "event_date_initiated": "2005-09-29",
      "event_date_posted": "2005-11-01",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-01-29",
      "res_event_number": "33707",
      "product_code": "MVC",
      "product_description": "K 520711-2, Hercep Test, 35Test, HER2, Protein",
      "code_info": "Lot number: 00016965, 100018107",
      "firm_fei_number": "2022180",
      "recalling_firm": "Dakocytomation California Inc",
      "address_1": "6392 Via Real",
      "city": "Carpinteria",
      "state": "CA",
      "postal_code": "93013-2921",
      "additional_info_contact": "Scot D. Kinghorn\n805-566-5478",
      "reason_for_recall": "Formulation error in the Visualization Reagent (vial 3) component contained in Hercep Test kits. The error was in the concentration of  Polyethylene Glycol contained in the formulation.",
      "root_cause_description": "Other",
      "action": "Notification letter dated Sept 29,2005 was sent by certified mail to consignees instructing disposal of product.",
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        "medical_specialty_description": "Unknown",
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