Device recall
Z-2530-2016: Perioscopy Sheath: Part number: 1008; The Perioscopy Sheath is a single-use…
FDA device recall · Class II · Danville Materials, Inc.
Key facts
| Recall number (Z-number) | Z-2530-2016 |
|---|---|
| Recall event | 74533 |
| Product | Perioscopy Sheath: Part number: 1008; The Perioscopy Sheath is a single-use sterile component used with the Perioscopy System, which is a medical device that features miniaturized digital video technology, and enables the healthcare professional to see magnified details of the tooth anatomy and… |
| Product code | EIA |
| Recalling firm | Danville Materials, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 9, 2016 |
| 510(k) numbers | K982480 |
| FEI number | 3002833004 |
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