{
  "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": [
    {
      "country": "United States",
      "city": "San Jose",
      "address_1": "5900 Optical Ct",
      "reason_for_recall": "The recalled products were shipped without the required temperature control packaging, therefore could potentially have been exposed to elevated temperatures during transit.",
      "address_2": "",
      "product_quantity": "155 devices",
      "code_info": "Serial/Lot Number(s) Affected:  4600: 15J456;  4601: 16A463, 16G470, 17F510;  4607: 16A461, 16D465, 16E467, 16F468, 17E506, 17E507;  4612: 16A458, 16A459, 17D489, 17E503, 17E504",
      "center_classification_date": "20180312",
      "distribution_pattern": "Netherlands",
      "state": "CA",
      "product_description": "CMI (Collagen Meniscus Implant) device, Ivy Sports Medicine s collagen-based meniscus implant    Product Usage:  The CMI device, Ivy Sports Medicine s collagen-based meniscus implant, is comprised primarily of bovine type I collagen (nominally 99%) derived from tendon and small quantities of glycosaminoglycans (GAGs: chondroitin sulfate and sodium hyaluronate). The device functions as a resorbable scaffold that is replaced by the patient s own tissue.The CMI device is designed to function as an absorbable template to facilitate host meniscus tissue regeneration in patients who have an irreparable meniscus tear or loss of meniscus tissue. The CMI meniscus tissue through the implant s absorption and replacement by patient s native tissue.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Stryker Corporation",
      "recall_number": "Z-0974-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79030",
      "more_code_info": "",
      "recall_initiation_date": "20180125",
      "postal_code": "95138-1400",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}