Recall database

Bone Wedge recalls

Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.

Showing 1–2 of 2 recalls

Class IIIOngoingZ-2972-2026

Paragon 28, Inc. recalls Custom Made Device Implant 6123 Navicular Cage Nominal Right Rev A

Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

Bone Wedge
Under Investigation by firm

Paragon 28, Inc.COAug 26, 2026

Class IIIOngoingZ-2971-2026

Paragon 28, Inc. recalls Custom Made Device Implant 6123 Navicular Cage Small Right Rev A

Device was recalled due to an elevated oxygen level in excess of the allowable limit. Elevated oxygen levels may contribute to reduced material ductility.

Bone Wedge
Under Investigation by firm

Paragon 28, Inc.COAug 26, 2026