{
  "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,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "The lidstock label incorrectly displays a  MR (Magnetic   Resonance ) Conditional  symbol (instead of a  MR Unsafe symbol) in reference to a component of the kit",
      "address_2": "",
      "product_quantity": "80 eaches",
      "code_info": "Lot/Batch Number: PMC 23F19H0224",
      "center_classification_date": "20200123",
      "distribution_pattern": "US distribution to SC",
      "state": "PA",
      "product_description": "Arrow Arterial Catherization Kit-20 Ga. x 4.45 cm Radiopaque Polyurethane over 22 Ga. TW Introducer Needle with Integral .018\" (0.46 mm) dia. Spring-Wire Guide  Product Code: ASK-04020-PMC     The Arrow¿ Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels.",
      "report_date": "20200129",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-0844-2020",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "84635",
      "more_code_info": "",
      "recall_initiation_date": "20191212",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}