{
  "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": [
    {
      "country": "United States",
      "city": "Grand Rapids",
      "address_1": "2710 Northridge Dr Nw",
      "reason_for_recall": "The pop-off valve in the defective devices remain open and a squeeze of the bag may not generate enough force to force the duck bill valve open and therefore no air will be delivered to the victim.",
      "address_2": "Suite A",
      "product_quantity": "251,384",
      "code_info": "Manual Resuscitator Bag Series:  AF1000, AF2000, AF5000, BT4000, VN2000,  VN5000, VT1000; Lot #s105147 -107609.  AF1000, AF2000, AF3000, AF4000, AF5000,  BT2000, BT3000, BT4000, PRO-1900, SC7000,  SC8120, SS3200, VN2000, VN3000, VN4000,  VN5000; Lot #s 106245 -107291.  VN2102; Lot #200349.  AF1000, AF2000, AF3000, AF4000, AF5000,  BT2000, BT3000, BT4000, BT5000, BVM700,  CPRM2000, CPRM3000, PRO-1000, PRO-2000,  SC7000, SC8020, VN2000, VN3000, VN4000; Lot #s 107029 -107634.  VN2002; Lot # 200492.  SC8000, SC9000; Lot #s 101441 -107461.  CPRM1000; Lot #s 99523 -107315.",
      "center_classification_date": "20140703",
      "distribution_pattern": "US Nationwide Distribution in the states of OH, NY, TX, TN, FL, CT, and VA,",
      "state": "MI",
      "product_description": "Manual Resuscitator Bag Series: AF1000, AF2000, AF3000, AF4000, AF5000, BT2000, BT3000, BT4000, BT5000, BVM700, CPRM1000, CPRM2000, CPRM3000, PRO-1900, PRO-1000, PRO-2000, SC7000, SC8000, SC8020, SC8120, SC9000, SS3200, VN2000, VN3000, VN4000, VN5000, VT1000 , VN2102,  VN2002.   Emergency manual resuscitator for the Pediatric Population.",
      "report_date": "20140709",
      "classification": "Class I",
      "openfda": {},
      "recalling_firm": "Ventlab LLC",
      "recall_number": "Z-1948-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68242",
      "termination_date": "20151117",
      "more_code_info": "",
      "recall_initiation_date": "20140516",
      "postal_code": "49544-9112",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}