{
  "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": [
    {
      "status": "Ongoing",
      "city": "Springfield",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "82499",
      "recalling_firm": "ROi Consolidated Service Center (CSC)",
      "address_1": "2909 N Neergard Ave",
      "address_2": "N/A",
      "postal_code": "65803-6317",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Distributed to LA and MO",
      "recall_number": "Z-2221-2019",
      "product_description": "Regard ¿ custom surgical pack labeled as \"LAPAROSCOPIC - OSU\" including recalled Stryker part numbers 0620 040 660 Pneumosure High Flow II Tubeset, 0620 040 690 Pneumosure Heated Tubeset with RTP and 0620 040 680 Pneumosure High Flow Tubeset with RTP.",
      "product_quantity": "312 packs",
      "reason_for_recall": "Resource Optimization & Innovation (ROi) has received a recall notice from Stryker regarding tube sets potentially detaching from the cassette, which can lead to leaking gas or a hissing sound.",
      "recall_initiation_date": "20190321",
      "center_classification_date": "20190808",
      "report_date": "20190814",
      "code_info": "Item Number (Lot Number, Expiration Date): 880341004 (043444D, 43566);    880341005 (047474E, 43706);  880341005 (049043E, 43750);"
    }
  ]
}