Device recall
Z-0012-2023: Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412
FDA device recall · Class II · Hobbs Medical, Inc.
Key facts
| Recall number (Z-number) | Z-0012-2023 |
|---|---|
| Recall event | 90769 |
| Product | Hobbs Medical Flex-Ez Guide Wire Disposable For endoscopy procedures Ref: 3412 |
| Product code | EYB |
| Recalling firm | Hobbs Medical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K914358 |
| FEI number | 1220592 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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