{
  "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": "Terminated",
      "city": "Mansfield",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "86554",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "15 Hampshire St Bldg 5",
      "address_2": "N/A",
      "postal_code": "02048-1113",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US Nationwide, Australia and Canada",
      "recall_number": "Z-0424-2021",
      "product_description": "Covidien MONOJECT Standard Hypodermic Needle, Polypropylene Hub 22 G x 3/4\". Intended use to facilitate activities such as: withdrawal of medication from a container, aspiration of fluid from a patient, injection of medication into a patient, and transfer fluids    Item Code: 8881250248",
      "product_quantity": "519,676 units",
      "reason_for_recall": "Potential for the needle to detach from the cartridge after the bottom of the cartridge is twisted and removed. If the needle is not securely seated, the needle can fall out of the sheath and cause the unused needle to project out of the cartridge, and  result in a needle stick/puncture from the clean/unused needle",
      "recall_initiation_date": "20200925",
      "center_classification_date": "20201105",
      "termination_date": "20231030",
      "report_date": "20201111",
      "code_info": "Lot Number: 011144    Expanded Recall 11/4/20:  Lot Number: 011145"
    }
  ]
}