Device recall
Z-1809-2013: Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a…
FDA device recall · Class II · Advanced Orthogonal Equipment, Incorporated
Key facts
| Recall number (Z-number) | Z-1809-2013 |
|---|---|
| Recall event | 65391 |
| Product | Advanced Orthogonal Percussion Adjusting Instrument Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra. |
| Product code | LXM |
| Recalling firm | Advanced Orthogonal Equipment, Incorporated |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 25, 2019 |
| 510(k) numbers | K946258 |
| FEI number | 3006315109 |
At a glance
- 1–9 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