{
  "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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      "product_res_number": "Z-0427-06",
      "event_date_initiated": "2005-10-14",
      "event_date_posted": "2006-01-24",
      "recall_status": "Terminated",
      "event_date_terminated": "2006-05-09",
      "res_event_number": "33923",
      "product_code": "JAY",
      "product_description": "Flexible Support Arm Assembly. Breathing Tube Support. Catalog number BE 122-30",
      "code_info": "Lot numbers PO902505 and PO900805",
      "firm_fei_number": "2518436",
      "recalling_firm": "Instrumentation Industries Inc",
      "address_1": "2990 Industrial Blvd",
      "city": "Bethel Park",
      "state": "PA",
      "postal_code": "15102-2536",
      "additional_info_contact": "Susan Mantia\n412-854-1133 Ext. 433",
      "reason_for_recall": "potential for the flexible tube portion of the assembly to become brittle and break",
      "root_cause_description": "Other",
      "action": "All customers (and/or end-users) were notified on October 14 and 17, 2005 by telephone.  Formal notification letters were sent (certified) to each customer (and/or end-user) on October 17 and 18, 2005.",
      "product_quantity": "22 units",
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