{
  "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": "2026-05-06",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "West Caldwell",
      "address_1": "23 Fairfield Pl",
      "reason_for_recall": "Ten units of Model EMV+ Devices were shipped out in error before the verification and validation was completed for a new integrated circuit (IC) on the CPU PCB.",
      "address_2": "",
      "product_quantity": "Ten Units",
      "code_info": "Serial numbers: VCDB120315, VCDB120316,  VCDB120299, VCDB120300, VCDB120313, VCDB120307, VCDB120312, VCDB120303, VCDB120310, VCDB120297.",
      "center_classification_date": "20120807",
      "distribution_pattern": "US Distribution to the state of Illinois.",
      "state": "NJ",
      "product_description": "Model 731 EMV+ Uni-Vent, Impact Instrumentation Inc., 27 Fairfield Place, West Caldwell NJ 07006. Indicated for use in the management of acute or chronic respiratory failure or during resuscitation by providing continuous positive -pressure ventilation.",
      "report_date": "20120815",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Impact Instrumentation, Inc.",
      "recall_number": "Z-2152-2012",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "62535",
      "termination_date": "20120815",
      "more_code_info": "",
      "recall_initiation_date": "20120319",
      "postal_code": "07006-6206",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}