{
  "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",
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      "product_res_number": "Z-0494-03",
      "event_date_initiated": "2002-12-06",
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      "recall_status": "Terminated",
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      "res_event_number": "25392",
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      "code_info": "All Lots.",
      "firm_fei_number": "2050012",
      "recalling_firm": "Beckman Coulter Inc",
      "address_1": "200 South Kraemer Blvd W 337",
      "city": "Brea",
      "state": "CA",
      "postal_code": "92822",
      "additional_info_contact": "Lynne McBride\n714-961-3626",
      "reason_for_recall": "Primary tube sampling issue may cause false low results.",
      "root_cause_description": "Other",
      "action": "Recall letters were sent to customers  on 12/6/2002 informing them to not process the sample directly from the primary collection tubes but to pour off a bit into a separate tube. Labs are to incorporate this into their Standard Operating Procedures until the firm can identify another resolution to the problem.",
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