Stryker Corporation recalls Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the

Recalled July 10, 2024 · FDA recall Z-2260-2024 · Stryker

Hazard

Expired Products distributed to customers · FDA Class II

Units

3 units

Sold at

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

Description

Expired Products distributed to customers

Product

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

Manufacturer(s)

Stryker Corporation

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →