{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "80734",
      "recalling_firm": "Valeris Medical, LLC",
      "address_1": "200 Cobb Pkwy N Bldg 200 Ste 210",
      "address_2": "N/A",
      "postal_code": "30062-3500",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to FL, OH, OK, and TX,  Foreign distribution was made to the United Kingdom and New Zealand.",
      "recall_number": "Z-0104-2019",
      "product_description": "Valeris Medical Apollo Medial Suture Anchor, Catalog Number MSA-4515, 4.5 x 15mm, each package contains (1) PEEK Screw, (1) #2 ForceBraid Blue, and (1) #2 ForceBraid White, 5 packages per container, Sterile, Rx.  The firm name on the label is Valeris Medical, Marietta, GA.",
      "product_quantity": "75 units",
      "reason_for_recall": "The product was mislabeled as containing the incorrect type of suture.",
      "recall_initiation_date": "20180716",
      "center_classification_date": "20181012",
      "termination_date": "20200804",
      "report_date": "20181024",
      "code_info": "Lot #1982, Exp. 3/22/2019"
    }
  ]
}