{
  "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,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "124595",
      "product_res_number": "Z-0744-2014",
      "event_date_initiated": "2013-12-16",
      "event_date_posted": "2014-01-14",
      "recall_status": "Terminated",
      "event_date_terminated": "2014-03-27",
      "res_event_number": "67043",
      "product_code": "MLR",
      "k_numbers": [
        "K023290",
        "K042116"
      ],
      "product_description": "STERRAD NX Sterilization System, Product Code: 10033\r\n\r\nThe STERRAD NX Sterilization System is a general purpose, low temperature sterilizer which uses the STERRAD NX process to inactivate microorganisms on a broad range of medical devices and surgical instruments.",
      "code_info": "not available",
      "firm_fei_number": "3003662624",
      "recalling_firm": "Advanced Sterilization Products",
      "address_1": "33 Technology Dr",
      "city": "Irvine",
      "state": "CA",
      "postal_code": "92618-2346",
      "additional_info_contact": "949-453-6400",
      "reason_for_recall": "Advanced Sterilization Products (ASP) is recalling the STERRAD NX, STERRAD 50, and STERRAD 100S Sterilization Systems because some healthcare workers detected odors or smells possibly emanating from STERRAD Systems.",
      "root_cause_description": "Under Investigation by firm",
      "action": "Advanced Sterilization Products (ASP) sent an Urgent Medical Device Field Safety Notification dated December 16, 2013, to all affected customers. The letter identified the product, the problem, and the action to be taken by the customer.  Customers were instructed to complete and return the customer response forms.  Customers with questions were also  instructed to contact ASP Professional Services directly at (888) 783-7723 and select option number 2.\r\nFor questions regarding this recall call 949-453-6400.",
      "product_quantity": "5584 units",
      "distribution_pattern": "Nationwide Distribution",
      "openfda": {
        "k_number": [
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        "device_name": "Sterilizer, Chemical",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.6860",
        "device_class": "2",
        "registration_number": [
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}