Device recall
Z-1729-2016: American Surgical Americot Blue 3/8" x 3/4" Ref Number: 20-14S Product Usage…
FDA device recall · Class II · American Surgical Company
Key facts
| Recall number (Z-number) | Z-1729-2016 |
|---|---|
| Recall event | 73734 |
| Product | American Surgical Americot Blue 3/8" x 3/4" Ref Number: 20-14S Product Usage: Neurosurgical and Nonneurosurgical Sponges |
| Product code | GDY |
| Recalling firm | American Surgical Company |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 21, 2016 |
| 510(k) numbers | K854714 |
| FEI number | 1221144 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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