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Paragon 28, Inc.

Paragon 28, Inc.: 2 recalls listed since July 2026 across FDA.

By year

  • 20262

By agency

  • FDA2

By category

  • Medical Device2

All recalls (2)

Paragon 28 Navicular Cage Foot Implants

The foot implant has elevated oxygen levels that may reduce material ductility.

Low risk, FDA, , Device defect

Paragon 28 Phantom Hindfoot TTC/TC Ball Tipped Guide Rod

The P28 Phantom Intramedullary Nail System guide rod has breaches in its sterile barrier.

Moderate risk, FDA, , Sterility problem
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