{
  "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": "Marquette",
      "address_1": "375 River Park Cir",
      "reason_for_recall": "Three lots of the Bullet -Tip VBR 13mm x 32 mm implants are mislabeled with a light green colored label, used for 16 mm trial instead of a lime green label, used for a 13 mm trial.",
      "address_2": "",
      "product_quantity": "18",
      "code_info": "Part Number: 32-13-32 Lot: 200827 Expiration Date: 2019-12-18  Part Number: 30-T-13-6 Lot: 202726 Expiration Date: 2020-01-16   Part Number: 30-T-1036-13-6 Lot: 202582 Expiration Date: 2020-01-15",
      "center_classification_date": "20150626",
      "distribution_pattern": "US Distribution to the states of : FL and NY",
      "state": "MI",
      "product_description": "Bullet-Tip PEEK VBR/IBF System, 32mm(l) 13mm(H) Implant 32-13-32 UDI (01)008464680341 08(17)191218(10)200827; T-Plus PEEK VBR/IBF System, 10mm(W) x 27mm(l) x 13mm(H) Implant, 6degree lordotic 30-T-13-6 UDI (01) 00846468032920(17) 200116(10) 202726; and T-Plus PEEK VBR/IBF System, 10mm(W) x 36 mm(l) x 13mm(H) Implant, 6degree lordotic 30-T-1036-13-6 UDI (01)00846468032760(17)200115(10)202582.                                                                                                                                      These products are part of the lnterbody Fusion Vertebral  Body Replacement System to ensure stability of the spine and adequate compression of the implant.",
      "report_date": "20150708",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)",
      "recall_number": "Z-1916-2015",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "71424",
      "termination_date": "20151029",
      "more_code_info": "",
      "recall_initiation_date": "20150521",
      "postal_code": "49855-1781",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}