Nextremity Solutions: Medical Device Recall in 2020 - (Recall #: Z-1458-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

Nextra Hammertoe Correction System-4.5MM Middle, 3.2MM Proximal, SS, Sterile. REF: NX-4532K - Product Usage: The Nextra Hammertoe Correction System is a system of implants and associated instruments which is indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toes.

Product Classification:

Class II

Date Initiated: February 12, 2020

Date Posted: March 18, 2020

Recall Number: Z-1458-2020

Event ID: 84924

Reason for Recall:

Proximal end of the driver in the affected product may be oversized in varying degrees, potentially making it difficult to connect with and remove from the proximal Nextra implant

Status: Terminated

Product Quantity: 190 units

Code Information:

Lot Number: 168117318B UDI: 00817701020011

Distribution Pattern:

International distribution in the countries of Spain, United Kingdom, Germany, and Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated