Device recall
Z-2052-2018: Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized…
FDA device recall · Class II · Hobbs Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2052-2018 |
|---|---|
| Recall event | 79903 |
| Product | Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained personnel through a flexible endoscope when brush cell samples are required for cytological analysis. |
| Product code | FDX |
| Recalling firm | Hobbs Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 10, 2020 |
| 510(k) numbers | K834402 |
| FEI number | 1220592 |
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