{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
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  "results": [
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      "cfres_id": "44063",
      "product_res_number": "Z-0667-06",
      "event_date_initiated": "2006-02-03",
      "event_date_posted": "2006-03-21",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-06-04",
      "res_event_number": "34545",
      "product_code": "MEA",
      "k_numbers": [
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      "product_description": "Stryker PainPump1 2-Site Y-Connector; Product number 500-250-000.",
      "code_info": "Lot 2005053102.",
      "firm_fei_number": "1811755",
      "recalling_firm": "Stryker Instruments Div. of Stryker Corporation",
      "address_1": "4100 E Milham Ave",
      "city": "Portage",
      "state": "MI",
      "postal_code": "49002-9704",
      "additional_info_contact": "800-800-4236 Ext. 3808",
      "reason_for_recall": "The catheter tubing included in the kit may break during removal.",
      "root_cause_description": "Other",
      "action": "Each consignee was notified of the recall via recall letter dated 2/7/06, which requested that they destroy the affected lots on site. International accounts were notified via email.",
      "distribution_pattern": "Nationwide, Australia and Canada.",
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        "device_name": "Pump, Infusion, Pca",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
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}