{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "37581",
      "product_res_number": "Z-0027-05",
      "event_date_initiated": "2005-02-24",
      "event_date_posted": "2005-03-23",
      "recall_status": "Terminated",
      "event_date_terminated": "2005-06-14",
      "res_event_number": "31276",
      "product_description": "Uterine Introducing Catheter 5F, 300 mm in length. The product is shipped in a sterile tyvek pouch",
      "code_info": "Lot number 741105 exp 11/07",
      "firm_fei_number": "1000121341",
      "recalling_firm": "Bioteque America Inc",
      "address_1": "340 E Maple Ave Ste 204c 340 E Maple Ave",
      "address_2": "Ste 204c",
      "city": "Langhorne",
      "state": "PA",
      "postal_code": "19047-2848",
      "additional_info_contact": "Denis Dorsey\n215-750-8072",
      "reason_for_recall": "product is marketed without a 510(k)",
      "root_cause_description": "Other",
      "action": "The recalling firm telephoned the distributors and sales representatives on 2/23/05 informing them of the problem and the need to return the product. As a follow up to the telephone call, a recall letter dated 2/24/05 was issued to the distributors.",
      "product_quantity": "115 units",
      "distribution_pattern": "The products were shipped to distributors in OH and MI. The product was also provided to sales representatives.",
      "openfda": {}
    }
  ]
}