{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Mahwah",
      "address_1": "800 Macarthur Blvd",
      "reason_for_recall": "The firm made multiple changes to the product requiring the submission of a new 510(k) premarket notification.",
      "address_2": "",
      "product_quantity": "1719",
      "code_info": "All Gas Modules 3 with Part Number 115-030108-00 purchased between February 14, 2008 and October 2015.",
      "center_classification_date": "20180328",
      "distribution_pattern": "Worldwide Distribution - U.S. Nationwide in the states: AK, AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA, WI, WY, including Puerto Rico and distributed to 30 foreign consignees.",
      "state": "NJ",
      "product_description": "Gas Module 3 monitoring spirometer, Part Number: 115-030108-00    Product Usage:  The Gas Module 3 is an accessory device designed to monitor airway gases during anesthesia and/or assisted respiration. Monitored gases includes O2, CO2, N2O and anesthetic agents Halothane, Isoflurane, Sevoflurane, Desflurane and Enflurane. It is intended for use in a fixed location such as the operating room or intensive care unit. The Gas Module 3 is compatible with Mindray patient monitors which display the gas analysis results through the use of a proprietary communication protocol.",
      "report_date": "20180404",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Mindray DS USA, Inc. dba Mindray North America",
      "recall_number": "Z-1242-2018",
      "initial_firm_notification": "Telephone",
      "product_type": "Devices",
      "event_id": "79423",
      "termination_date": "20180829",
      "more_code_info": "",
      "recall_initiation_date": "20171201",
      "postal_code": "07430-2001",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}