Device recall
Z-2540-2020: FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Usage: intended to…
FDA device recall · Class II · FHC, Inc.
Key facts
| Recall number (Z-number) | Z-2540-2020 |
|---|---|
| Recall event | 85897 |
| Product | FHC Guideline 4000 5.0 GL5 Main Processing Unit - Product Usage: intended to record and stimulate electrophysiological activity, as well as aid in the accurate placement of electrodes and other instruments. Catalogue Number: C0215 UDI: 00873263006740 |
| Product code | GZL |
| Recalling firm | FHC, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2020 |
| 510(k) numbers | K183123 |
| FEI number | 3002250546 |
At a glance
- 1–9 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