{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "One lot of product is from product code AK-22502 so it contains a 2-lumen, 5 Fr x 5 cm  catheter. However, this product is incorrectly labeled as AK-25502, so the lidstock says it  contains a 2-lumen, 5 Fr x 8 cm catheter. No patient injuries have been reported related to this  issue.",
      "address_2": "",
      "product_quantity": "166",
      "code_info": "13F17K0202",
      "center_classification_date": "20180822",
      "distribution_pattern": "Distributors in MO and UT. Medical facilities in AL, CA, IL, MA, NH, NM, NY, TX, VA, and WI.",
      "state": "PA",
      "product_description": "Pediatric Two-Lumen Central Venous  Catheterization Kit with Blue FlexTip  ARROWg+ard Blue Catheter, Cat. No. AK-22502     Product Usage:  The multiple-lumen catheter permits venous access to the central circulation of pediatric patients. The ARROWg+ard antimicrobial surface is intended to help provide protection against catheterrelated infections. The catheter is not intended to be used as a treatment for existing infections, nor is it indicated for long-term use. The use of the 4, 5, and 5.5 Fr. antimicrobial surface catheters in infants weighing less than 2.0, 2.5, and 3.0 kilograms respectively, have not been evaluated. Therefore, the benefits of these catheters in infants weighing less than the indicated weights should be weighed against any possible risks.",
      "report_date": "20180829",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2886-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80631",
      "termination_date": "20200429",
      "more_code_info": "",
      "recall_initiation_date": "20180703",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}