{
  "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": "San Carlos",
      "state": "CA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67492",
      "recalling_firm": "Biocardia, Inc.",
      "address_1": "125 Shoreway Rd Ste B",
      "address_2": "",
      "postal_code": "94070-2718",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Telephone",
      "distribution_pattern": "US Distribution including the states of FL, MA, WY. OH, MI and KS.",
      "recall_number": "Z-0991-2014",
      "product_description": "MORPH ACCESSPRO Steerable Introducer;  6F introducer, 90 cm working length:  Sterile in unopened, undamaged pouch. Sterilized by EtO gas, Non-pyrogenic:  BioCardia Inc.  San Carlos, CA 94070    Intended to provide a pathway through which medical instruments such as balloon dilation catheters, guidewires and other therapeutic devices may be introduced into the peripheral vasculature.",
      "product_quantity": "11 units",
      "reason_for_recall": "Tyvek packaging may be worn, causing loss of package integrity.",
      "recall_initiation_date": "20140207",
      "center_classification_date": "20140219",
      "termination_date": "20140403",
      "report_date": "20140226",
      "code_info": "Catalog number MAP690; Lot numbers 01162 and 01186.",
      "more_code_info": ""
    }
  ]
}