Paragon 28, Inc.: Medical Device Recall in 2022 - (Recall #: Z-1468-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

HammerTube Implant, 2.75mm, 10¿ Cannulated (Sterile)

Product Classification:

Class II

Date Initiated: May 26, 2022

Date Posted: August 3, 2022

Recall Number: Z-1468-2022

Event ID: 90436

Reason for Recall:

Due to Titanium plasma coating not present implant.

Status: Ongoing

Product Quantity: 9 implants

Code Information:

Part Number: P40-002-0275-S UDI-DI Code: (01)00889795033987(17)270323(10)26010822202 Lot Number: 26010822202

Distribution Pattern:

U.S. Nationwide distribution in the states of AL, CA, GA, IL and KY.

Voluntary or Mandated:

Voluntary: Firm initiated