{
  "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": "Ongoing",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "88421",
      "recalling_firm": "Cardinal Health",
      "address_1": "777 West St",
      "address_2": "N/A",
      "postal_code": "02048-1122",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide Distribution: \u0013 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, PI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY.",
      "recall_number": "Z-2286-2021",
      "product_description": "Monoject 0.9% Sodium Chloride Flush Syringe, 5mL Fill, STERILE, Product Code 8881570125     The proposed device is indicated for use in flushing compatible intravenous tubing systems and indwelling intravascular access devices.",
      "product_quantity": "267,217,860 eaches in total",
      "reason_for_recall": "Potential for the plunger to draw back after the air has been expelled and reintroduce air back into the syringe.",
      "recall_initiation_date": "20210804",
      "center_classification_date": "20210821",
      "report_date": "20210901",
      "code_info": "20D0614  21D0894  20D0624  20D0674  20D0684  20H1504  20H1514"
    }
  ]
}