{
  "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-1215-2020",
      "product_description": "EPIDURAL CATHETERIZATION KIT, Product Code UR-05501-EXP",
      "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: 71F19B0757  71F19D1493  71F19E2344  71F19G2640  71F19J0575  71F19C0748  71F19E0193  71F19G1146  71F19H2120  71F19K1689",
      "more_code_info": ""
    }
  ]
}