FDA Device recall 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…
- FDA Device
- Class II
- ongoing
- Published 2024-07-10
On 2024-07-10 the FDA classified a Class II recall of Curved, super elastic cement delivery needle that passes through the cannula in a straight configuration and enters the vertebral body in a… by Stryker, citing expired Products distributed to customers.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2260-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2024-06-03 |
| Published | 2024-07-10 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Stryker |
| Distribution | US |
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
Expired Products distributed to customers
Identifiers
| code_info | GTIN: 07613327374629 Lot Number: 6659783 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2260-2024%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.