{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Arrow International is notifying each customer who received the affected that product that the kits do not contain important information regarding the 3M Tegaderm CHG Chlorhexidine Gluconate I.V. Securement Dressing.",
      "address_2": "",
      "product_quantity": "3,918 units",
      "code_info": "ASK-04001-DU9 and ASK-04001-DU10  Device Listing Number D156491  Lot Numbers:  23F15L0593  23F16A0300  23F16B0028  23F16B0523  23F16J0151  23F16K0363  23F16K0431  23F16K0820  23F15L0662  23F16A0298  23F16B0338  23F16C0321  23F16C0632  23F16J0105  23F16K0449",
      "center_classification_date": "20170526",
      "distribution_pattern": "US Distribution to the state of : NC",
      "state": "PA",
      "product_description": "Arrow(R) VPS(R) Access Kit for use with 4 and 5 Fr. Peripherally Inserted Central Venous Catheters",
      "report_date": "20170607",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2170-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "77163",
      "termination_date": "20180803",
      "more_code_info": "",
      "recall_initiation_date": "20170428",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}