{
  "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",
    "results": {
      "skip": 0,
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  "results": [
    {
      "cfres_id": "43940",
      "product_res_number": "Z-0584-06",
      "event_date_initiated": "2006-01-17",
      "event_date_posted": "2006-03-07",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-02-05",
      "res_event_number": "34494",
      "product_code": "MEB",
      "k_numbers": [
        "K052117",
        "K932740"
      ],
      "product_description": "Easypump ST 100-1  infusion pump",
      "code_info": "lot 562791",
      "firm_fei_number": "3011270181",
      "recalling_firm": "I-Flow Corporation",
      "address_1": "20202 Windrow Dr",
      "city": "Lake Forest",
      "state": "CA",
      "postal_code": "92630-8152",
      "additional_info_contact": "Shane Noehre\n949-202-2653",
      "reason_for_recall": "The sterile pack may contain the wrong infusion pump inside.",
      "root_cause_description": "Other",
      "action": "The affected customer has been notified with a Notification letter dated January 17, 2006 via e-mail of Recall Notification Letter, with follow-up confirmation e-mails.",
      "product_quantity": "630",
      "distribution_pattern": "France only",
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        "device_name": "Pump, Infusion, Elastomeric",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
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    }
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}