Stryker Spine: Medical Device Recall in 2023 - (Recall #: Z-0610-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2023.

Data Source: FDA.

Product Description:

LITe Decompression Snake Arm, REF 48080230

Product Classification:

Class II

Date Initiated: November 1, 2023

Date Posted: December 27, 2023

Recall Number: Z-0610-2024

Event ID: 93573

Reason for Recall:

Product arm was manufactured with the incorrect clamp component. As a result, the affected product arm cannot attach to the arm post shaft.

Status: Ongoing

Product Quantity: 9

Code Information:

UDI-DI (GTIN): 07613327263909, lot # 227764.

Distribution Pattern:

US: MD, MI, NM, TX & OUS: Canada & France.

Voluntary or Mandated:

Voluntary: Firm initiated