Stryker Spine: Medical Device Recall in 2024 - (Recall #: Z-3210-2024)

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:

AVS Anchor-C Cervical Cage System Instructions For Use (IFU)- eIFU (revision 5)-Indicated for anterior cervical interbody fusion procedures in skeletally mature patients with cervical disc disease at one level from the C2-C3 disc to the C7-T1 disc.

Product Classification:

Class II

Date Initiated: August 23, 2024

Date Posted: October 2, 2024

Recall Number: Z-3210-2024

Event ID: 95274

Reason for Recall:

Labeling Correction: Instructions For Use (IFU)-Updated electronic Rev 5, specific language for indications for use for the United States and Canada was inadvertently removed.

Status: Ongoing

Product Quantity: 8,589 units

Code Information:

electronic eIFU (revision 5) Rev 5 available January 2023 to present.

Distribution Pattern:

Worldwide distribution - US Nationwide and the country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated