Class II

Medical Device Recall: 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 abil

Stryker Corporation · June 3, 2024

Reason for Recall

Expired Products distributed to customers

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

Distribution

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

States Affected

NATIONWIDE

Quantity Affected

3 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-2260-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Stryker Corporation Medical Device Recall: 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 abil | SafeCheck