Device recall
Z-1077-06: Zinnanti Injector - 2.0; Size 2.0 mm, Length 23 cm, latex free, single-use…
FDA device recall · Class II · Catheter Research, Inc
Key facts
| Recall number (Z-number) | Z-1077-06 |
|---|---|
| Recall event | 35241 |
| Product | Zinnanti Injector - 2.0; Size 2.0 mm, Length 23 cm, latex free, single-use, sterile. For in-office or hospital use when efficient sealing of the uterine cervix is required for the injection of liquid or gas such as hysterosalpingography, salpingoplasties, hydrotubation and Rubin''s test. REF… |
| Product code | LKF |
| Recalling firm | Catheter Research, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 4, 2007 |
| 510(k) numbers | K020292 |
| FEI number | 3008998256 |
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