Device recall
Z-0828-03: Dr. Fog Endoscopic Fog Prevention Kit; model DF-3120. Each box contains 40…
FDA device recall · Class II · Aspen Surgical Products, Inc.
Key facts
| Recall number (Z-number) | Z-0828-03 |
|---|---|
| Recall event | 26188 |
| Product | Dr. Fog Endoscopic Fog Prevention Kit; model DF-3120. Each box contains 40 packages. Each package contains one Dr. Fog treated sponge. |
| Product code | GCJ |
| Recalling firm | Aspen Surgical Products, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 13, 2003 |
| 510(k) numbers | K932449 |
| FEI number | 3002750084 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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