{
  "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": [
    {
      "status": "Terminated",
      "city": "Malvern",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "63204",
      "recalling_firm": "Orthovita, Inc., dBA Stryker Orthobiologics.",
      "address_1": "45 Great Valley Pkwy",
      "address_2": "N/A",
      "postal_code": "19355-1302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA Nationwide Distribution in the states of AZ, CA, CO, CT, DE, FL, GA, HI, IL, IN, KS, KY, LA, MD, ME, MI, MO, NC, ND, NH, NJ, NY, OH, OK, PA, RI, SC, TN, TX, UT, VA, WA, and WI.",
      "recall_number": "Z-1399-2013",
      "product_description": "Stryker Orthobiologics Aliquot Delivery System Manual Surgical Instrument - Aliquot Catheter, 6\", Part Number 2110-0503    Product Usage:  Facilitate placement of bone cement in weakened or diminished bone",
      "product_quantity": "69",
      "reason_for_recall": "There have been a few reported cases of the catheter breaking when removing the Aliquot catheter from the needle during vertebroplasty procedures.  This has been attributed to bending of the catheter during the retraction from the needle.  It was determined to be use errors.  The correction is limited to a revision of the Directions for Use.",
      "recall_initiation_date": "20121110",
      "center_classification_date": "20130524",
      "termination_date": "20141029",
      "report_date": "20130605",
      "code_info": "Manufacturer Part Number 2110-0503, Lot Numbers E908003R and E908002"
    }
  ]
}