Zimmer Biomet Spine Inc.: Medical Device Recall in 2024 - (Recall #: Z-0639-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

Vitality Polyaxial Screw, 7.5mmx 50mm, REF: 07.02000.118, used with Vitality and Vital Spinal Fixation System

Product Classification:

Class II

Date Initiated: October 16, 2023

Date Posted: January 10, 2024

Recall Number: Z-0639-2024

Event ID: 93650

Reason for Recall:

Spinal fixation system 7.5mmx 50mm screws are packaged with the correct labeling, but the screws themselves were laser marked with an incorrect size description of 7.5 x 40; use of incorrect screws could lead to screw perforation and indention of vascular or other structures.

Status: Ongoing

Product Quantity: 3

Code Information:

UDI-DI: 00889024002159, Lot: W834061

Distribution Pattern:

US Nationwide distribution in the states of MN, NE.

Voluntary or Mandated:

Voluntary: Firm initiated