FDA recall Z-2260-2024

Stryker Corporation · Class II · device

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

Reason for recall

Expired Products distributed to customers

Distribution

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

Key facts

Status
Ongoing
Initiation date
2024-06-03
Report date
2024-07-10
Voluntary/Mandated
Voluntary: Firm initiated
Location
Portage, MI, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2260-2024