{
  "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": [
    {
      "cfres_id": "49359",
      "product_res_number": "Z-0244-2007",
      "event_date_initiated": "2006-10-31",
      "event_date_posted": "2006-12-05",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-11-30",
      "res_event_number": "36788",
      "product_code": "BYW",
      "product_description": "Rusch (Latex Free) Neoprene Pecan Shaped Breathing Bag with 15 mm neck insert, size 1 liter; a rebreathing bag; Teleflex Medical, Bannockburn, IL 60015 USA, Made in UK",
      "code_info": "Catalog Number (REF) 21176AP, lot number 070318-1",
      "firm_fei_number": "3004959265",
      "recalling_firm": "Teleflex Medical",
      "address_1": "2345 Waukegan Rd Ste 120 2345 Waukegan Rd",
      "address_2": "Ste 120",
      "city": "Bannockburn",
      "state": "IL",
      "postal_code": "60015-1580",
      "additional_info_contact": "Ms. Julie McDowell \n610-948-2836",
      "reason_for_recall": "Mislabeling-The rebreathing bag is incorrectly labeled as a 1 liter bag when it is actually a 1/2 liter bag.",
      "root_cause_description": "Other",
      "action": "Teleflex Medical sent Urgent Medical Device Recall letters dated 10/31/06 via UPS overnight to the direct accounts, informing them that the product was incorrectly labeled as a 1 liter bag when the correct volume of the bag is  liter, and requesting that they cease use of the affected units and destroy them.  If the accounts further distributed the product, they were requested to conduct a sub-recall of the affected units from their customers. The accounts were instructed to complete and return by fax the enclosed Acknowledgement & Stock Status Form, indicating the number of units destroyed and if they are requesting replacement product. Any questions were directed to Linda Todd at 1-800-334-9751, ext. 4951.",
      "product_quantity": "50 bags",
      "distribution_pattern": "Nationwide including the states of California and Florida",
      "openfda": {
        "k_number": [
          "K895274",
          "K802165"
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        "registration_number": [
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        "device_name": "Device, Rebreathing",
        "medical_specialty_description": "Anesthesiology",
        "regulation_number": "868.5675",
        "device_class": "1"
      }
    }
  ]
}