Stryker Corporation: Medical Device Recall in 2024 - (Recall #: Z-2260-2024)

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:

Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a curved configuration. This provides physicians with the ability to inject bone cement into multiple different areas through a single point of access in the patient. Catalog Number: 1025-011-500

Product Classification:

Class II

Date Initiated: June 3, 2024

Date Posted: July 10, 2024

Recall Number: Z-2260-2024

Event ID: 94755

Reason for Recall:

Expired Products distributed to customers

Status: Ongoing

Product Quantity: 3 units

Code Information:

GTIN: 07613327374629 Lot Number: 6659783

Distribution Pattern:

US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.

Voluntary or Mandated:

Voluntary: Firm initiated