Drug recall
TRESTLE LUXE¿ Anterior Cervical Plating System, Product code KWQ. 510(k) K102820. The TRESTLE LUXE Anterior…
FDA recall event 51437 · Class II · Alphatec Spine, Inc.
Key facts
| Event ID | 51437 |
|---|---|
| Recall numbers | Z-2273-2012 |
| Recalling firm | Alphatec Spine, Inc. |
| Product type | Devices |
| Products | TRESTLE LUXE¿ Anterior Cervical Plating System, Product code KWQ. 510(k) K102820. The TRESTLE LUXE Anterior Cervical Plating System is a temporary device used to stabilize the cervical spine during… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | On May 9th 2012 Alphatec Spine received a complaint which reported that the distal tip of the Trestle Luxe Slide Alignment Tool (Part Number 71721), does not properly fit into the hexalobe screw on… |
| Initiation date | May 29, 2012 |
| Report date | Sep 5, 2012 |
| Termination date | Sep 4, 2012 |
| City | Carlsbad |
| State | CA |
| Country | United States |
| FEI number | 2027467 |
At a glance
- 1–9 Products in this recall
- 10–99 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: