{
  "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",
    "results": {
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      "product_res_number": "Z-0023-05",
      "event_date_initiated": "2004-08-17",
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      "recall_status": "Terminated",
      "event_date_terminated": "2004-10-19",
      "res_event_number": "29864",
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      "code_info": "Serial numbers 040639739, 040639849, 040639737, 040639738, 040639675, 040639674, 040639670, 040639671, 040639672, 040639716, 040639847, 040639848, 040639935, 040639936 and 040639937.",
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      "address_1": "6300 Sprinkle Rd",
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      "state": "MI",
      "postal_code": "49001",
      "additional_info_contact": "Renata Sila\n269-324-6689",
      "reason_for_recall": "Locking pins may be installed backward, and cot may drop from highest to lowest position when the users are not prepared for the drop.",
      "root_cause_description": "Other",
      "action": "Service representatives visited each customer, inspected the cots, and reinstalled the lock pins, if required, beginning on August 10, 2004.",
      "product_quantity": "15",
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