{
  "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": [
    {
      "country": "United States",
      "city": "Franklin Lakes",
      "address_1": "1 Becton Dr",
      "reason_for_recall": "The products have the potential to leak between the connection of the male luer lock and the yellow striped tubing.",
      "address_2": "",
      "product_quantity": "566,737 total",
      "code_info": "Batch numbers: 16127933  17017602  17055977  17117153  17125385  18015788",
      "center_classification_date": "20181103",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of:  AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MO, MT, NC, NE, NJ, NV, NY, OH, OR, PA, SC, TN, TX, UT, VA, WA, WI, WV, and Guam.    The products were distributed to the following foreign countries: Canada, United Arab Emirates and Saudi Arabia.",
      "state": "NJ",
      "product_description": "PCEA Kit ASV Yellow Stripe Microbore, Catalog Number 10800177    Product Usage:  PCEA Administration Set. Microbore tubing with Yellow Identification Stripe. Anti-siphon valve.   Set cannot be used for gravity infusion 1. Connect PCA syringe to female luer on administration set. 2. Push on syringe plunger to prime set. 3. Refer to PCA module directions for Use for complete loading and operating instructions. Notes:   The set should be changed according to the facility protocol or in accordance with currently recognized guidelines for IV therapy.   Antisiphon sets cannot be primed by gravity.",
      "report_date": "20181114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Becton Dickinson & Company",
      "recall_number": "Z-0387-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "81181",
      "termination_date": "20200413",
      "more_code_info": "",
      "recall_initiation_date": "20180926",
      "postal_code": "07417-1815",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}