Device recall
Z-1038-2023: Turbett Surgical Container, TS1000: Indicated for enclosing other medical…
FDA device recall · Class II · Turbett Surgical, Inc.
Key facts
| Recall number (Z-number) | Z-1038-2023 |
|---|---|
| Recall event | 91314 |
| Product | Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider |
| Product code | FRG |
| Recalling firm | Turbett Surgical, Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K153025 |
| FEI number | 3012421755 |
At a glance
- 1–9 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