{
  "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": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "84726",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "The products were distributed to the following US states:  AK, AR, AZ, CA, CO, CT, FL, GA, ID, IL, IN, LA, MA, MD, MI, MN, MO, MT, NC, NE, NH, NJ, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, and WY.",
      "recall_number": "Z-1181-2020",
      "product_description": "Epidural Catheterization Kit with FlexTip Plus, Open Tip, Single-  Port Catheter, Product Code ASK-05502-NY",
      "product_quantity": "343,105 total",
      "reason_for_recall": "There is the potential for various failures with the LOR (loss of resistance) syringes included in the kits resulting in dural puncture with some also requiring a blood patch.",
      "recall_initiation_date": "20200115",
      "center_classification_date": "20200213",
      "termination_date": "20230317",
      "report_date": "20200219",
      "code_info": "Lots: 23F19C0385  23F19G0310  23F19H0234  23F19K0248  23F19F0167  23F19G0434  23F19J0063",
      "more_code_info": ""
    }
  ]
}