{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Pittsburgh",
      "address_1": "2500 Jane St Ste 1",
      "reason_for_recall": "CME America BodyGuard 323 Infusion Pumps (recalled by manufacturer) is a component  to the Hemolung for EUA, and the infusion pump may have a delivery inaccuracy",
      "address_2": "",
      "product_quantity": "101 units",
      "code_info": "Serial Numbers:  A11530  A11531  A11532  A11533  A11534  A11535  A11536  A11537  A11538  A11539  A11541  A11543  A11544  A11545  A11546  A11548  A11552  A11553  A11554  A11555  A11556  A11557  A11561  A11562  A11563  A11565  A11566  A11567  A11568  A11569  A11570  A11571  A11572  A11573  A11575  A11576  A11577  A11578  A11579  A11580  A11581  A11582  A11583  A11584  A11585  A11586  A11587  A11590  A11591  A11592  A16164  A16794  A16795  A16796  A16797  A16798  A16799  A16800  A16801  A16802  A16803  A16804  A16805  A16806  A16807  A16808  A16809  A16810  A16811  A16812  A16813  A16814  A16815  A16816  A16817  A16818  A16819  A16820  A16821  A16822  A16823  A16824  A16825  A16826  A16827  A34951  A34952  A34953  A34954  A34955  A34957  A34958  A34960  A34961  A34962  A34963  A34964  A34965  A34967  A34969  A34970",
      "center_classification_date": "20210129",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "PA",
      "product_description": "ALung Technologies Hemolung Respiratory Assist System (RAS) with CME BodyGuard 323 Infusion Pump(EUA) - Product Usage: an off-the-shelf infusion pump and administration set to provide a 30 mL/hr continuous saline flush to the integrated blood pump bearing.",
      "report_date": "20210210",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alung Technologies Inc",
      "recall_number": "Z-0938-2021",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "87048",
      "termination_date": "20210517",
      "more_code_info": "",
      "recall_initiation_date": "20201218",
      "postal_code": "15203-2216",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}