Health & Personal Care
HIGH
FDA DEVICE
Paragon 28 Phantom Fibula Nail Recall 2025 for 20 Units Nationwide
Paragon 28 recalled 20 Phantom Fibula Nails nationwide after finding out-of-spec thread depths. The defect may prevent the nail from mating properly with the mounting bolt. Surgery could be aborted if the implant cannot mate with instrumentation. Hospitals and surgeons should stop using the device immediately and follow recall instructions.
Paragon 28
Fibula nail