{
  "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": [
    {
      "status": "Completed",
      "city": "Medina",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86788",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "711 Park Ave",
      "address_2": "N/A",
      "postal_code": "14103-1036",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic Distribution: ST, AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY and  Puerto Rico.  International Distribution: Canada, Barbados, Bermuda, St. Thomas, Guyana,   Trinidad and Tobago, Jamaica and Nassau Bahamas.",
      "recall_number": "Z-1150-2021",
      "product_description": "Infusion Pump",
      "product_quantity": "589,704 total units",
      "reason_for_recall": "Battery performance issues related to prolonged storage.",
      "recall_initiation_date": "20210106",
      "center_classification_date": "20210225",
      "report_date": "20210303",
      "code_info": "Infusion Pump Product codes:  35700ABB,  35700BAX, and  35700BAX2   Battery codes:  35083, 35162, 35195, and 35724.    Infusion Pump Product codes:  35700ABB,  35700BAX,  35700BAX2  3570009    Battery codes:  35223 and 36010"
    }
  ]
}