Device recall
Z-1360-2012: Removal of Literature/Brochures for Antalgic-Trak. "***What is…
FDA device recall · Class II · Spinetronics, LLC
Key facts
| Recall number (Z-number) | Z-1360-2012 |
|---|---|
| Recall event | 61234 |
| Product | Removal of Literature/Brochures for Antalgic-Trak. "***What is Antalgic-Trak?***Articulating Non-Surgical Spinal Decompression****Antalgic-Trak By Spinetronics***Note: "Decompression" as used herein refers to unloading due to distraction and positioning.***Antalgic-Trak is an improved form of… |
| Product code | ITH |
| Recalling firm | Spinetronics, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2012 |
| FEI number | 3006746551 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database