{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
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  "results": [
    {
      "country": "United States",
      "city": "Dallas",
      "address_1": "1420 Lakeside Parkway",
      "reason_for_recall": "Labeling: Incorrect or missing Lot and/or Exp Date:The Kit is incorrectly labeled as expiring May 2018 however the correct expiration date is May 2019.   In addition, device component (syringe) lacks 510(k) clearance.",
      "address_2": "",
      "product_quantity": "747 kits",
      "code_info": "LOT # ASM0020274 Exp 5/31/2018",
      "center_classification_date": "20190116",
      "distribution_pattern": "Nationwide in the USA",
      "state": "TX",
      "product_description": "Curaplex Epi Safe Kit, Rx Only, contains: 1mL Vial of Epinephrine, 1 Epi-Safe Syringe, 1 Safety needle, 2 Alcohol Prep Pads,1 Adhesive Dressing, 1 Insert. Distributed by Sarnova, HC. LLC's family companies: Bound Tree Medical. LLC, Cardio Partners, Inc., Emergency Medical Products, Inc. & Tri-amin Health Services, Inc. 5000 Tuttle Crossing Blvd, Dublin, OH 43016. Model 8600-01101",
      "report_date": "20190123",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Bound Tree Medical, LLC",
      "recall_number": "D-0379-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "81487",
      "termination_date": "20200511",
      "more_code_info": "",
      "recall_initiation_date": "20181101",
      "postal_code": "75208",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}