Nextremity Solutions: Medical Device Recall in 2022 - (Recall #: Z-0740-2022)

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:

Nextra Cannulated Hammertoe Standard Instrument Kit-indicated for small bone reconstruction limited to inter-digital repair and fusion of the lesser toe SKU: CH-STD-KT

Product Classification:

Class II

Date Initiated: January 13, 2022

Date Posted: March 16, 2022

Recall Number: Z-0740-2022

Event ID: 89588

Reason for Recall:

During insertion of the middle phalanx implant into bone, the driver may deform the implant locking mechanism and result in inadequate mating force between the middle and proximal phalanx implants, resulting in surgical delay, in-situ removal of the implant, use of alternative surgical approach, disassembly of the implants post-operatively, and revision

Status: Terminated

Product Quantity: 24 units

Code Information:

Lot Numbers: 1574701, 158961 UDI: 00817701026372

Distribution Pattern:

US Nationwide distribution in the states of AZ, IL, GA, LA, MD, NY, PA, TX, WA.

Voluntary or Mandated:

Voluntary: Firm initiated