Device recall
Z-0325-2023: Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1
FDA device recall · Class II · Busse Hospital Disposables, Inc.
Key facts
| Recall number (Z-number) | Z-0325-2023 |
|---|---|
| Recall event | 91079 |
| Product | Busse JOINT INJECTION TRAY -Intended as a nerve block REF No. 8561 R1 |
| Product code | OGJ |
| Recalling firm | Busse Hospital Disposables, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 2433012 |
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