Device recall
Z-2531-2018: Access Hi-Low Exam Tables, Model 6501-XX
FDA device recall · Class II · Brewer Company, LLC
Key facts
| Recall number (Z-number) | Z-2531-2018 |
|---|---|
| Recall event | 80164 |
| Product | Access Hi-Low Exam Tables, Model 6501-XX |
| Product code | LGX |
| Recalling firm | Brewer Company, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 29, 2019 |
| FEI number | 2182536 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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