FDAFDA · Food and drugs·Recall number Z-2260-2024
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
Published July 10, 2024 · Recall initiated: June 3, 2024
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Expired Products distributed to customers
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Stryker Corporation
- Distributor
- US Nationwide distribution in the states of Arkansas, California, Colorado, Florida, Michigan.
- Lot
- GTIN: 07613327374629 Lot Number: 6659783
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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