{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "64971",
      "recalling_firm": "Carefusion 2200 Inc",
      "address_1": "1500 S Waukegan Rd",
      "address_2": "Mpwm Bldg.",
      "postal_code": "60085-6728",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide in the states of AZ, CA, CO, DE, FL, GA, IL, LA, MA, MD, MI, MN, MO, MS, NC, NJ, NM, NY, OH, PA, TX, UT, WA",
      "recall_number": "Z-1947-2013",
      "product_description": "1) Adult Manual Resuscitator, 2K8004, Oxygen Reservoir Bag, Adult Mask;   2) Adult Manual Resuscitator, 2K8005, 40\" (1.0 m) Oxygen Reservoir Tubing, Adult Mask;   3) Adult Manual Resuscitator, 2K8017, Variable Volume Oxygen Reservoir Tubing, Adult Mask;   4) Adult Manual Resuscitator, 2K8034, 40\" (1.0 m) Oxygen Reservoir Tubing, PEEP Valve, without Mask;   5) Adult Manual Resuscitator, 2K8035, Oxygen Reservoir Bag, PEEP Valve, Adult Mask;   6) Pediatric Manual Resuscitator, 2K8037, 40\" (1.0 m) Oxygen Reservoir Tubing, PEEP Valve, Pediatric Mask, Pressure Limiting Valve with Lock;   7) Infant Manual Resuscitator, 2K8040, Oxygen Reservoir Bag, PEEP Valve, Infant Mask, Pressure Limiting Valve with Lock    Product Usage:  Pulmonary resuscitation",
      "product_quantity": "14,112 units",
      "reason_for_recall": "CareFusion has received four (4) customer reports of a component (oxygen connector) within the resuscitation bag being occluded which disables the flow of supplemental oxygen to the resuscitation bag and thus may pose a serious patient safety risk.",
      "recall_initiation_date": "20130422",
      "center_classification_date": "20130813",
      "termination_date": "20150616",
      "report_date": "20130821",
      "code_info": "1) Product Code 2K8005; Lot Numbers: 0000355656, 0000355659, 0000355662, 0000355664, 0000355665, 0000355666, 0000355668;   2) Product Code 2K8004; Lot Number: 0000355673;   3) Product Code 2K8017; Lot Numbers: 0000355676, 0000355677;   4) Product Code 2K8034; Lot Number: 0000355688;   5) Product Code 2K8035; Lot Number: 0000358023;   6) Product Code 2K8037; Lot Number: 0000358025;   7) Product Code 2K8040; Lot Number: 0000358026",
      "more_code_info": ""
    }
  ]
}