{
  "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": "Middleburg Heights",
      "address_1": "6753 Engle Rd",
      "reason_for_recall": "Product design change did not receive proper premarket clearance and lacks a 510 (k)",
      "address_2": "",
      "product_quantity": "",
      "code_info": "All Serial Numbers/Lots",
      "center_classification_date": "20190515",
      "distribution_pattern": "Domestically to AL, AR, AZ, CA, CO, FL, GA, IA, IL, IN, KS, KY, LA, MA, MD, MI, MO, MS, MT, NC, NE, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TN, KY, TX, UT, VA, WA, WI & WY    Internationally to Canada",
      "state": "OH",
      "product_description": "MediPress pneumatic compression system Full Arm (Medium)-Segmental Gradient, Model #6104M-S",
      "report_date": "20190522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Compass Health Brands (Corporate Office)",
      "recall_number": "Z-1345-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82629",
      "termination_date": "20201026",
      "more_code_info": "",
      "recall_initiation_date": "20190408",
      "postal_code": "44130-7934",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}