Device recall
Z-0592-2015: PKG, BIPOLAR FORCEPS, MICRO TIP, 45CM, P/N 0250080115 nationwide in US and…
FDA device recall · Class II · Stryker Endoscopy
Key facts
| Recall number (Z-number) | Z-0592-2015 |
|---|---|
| Recall event | 69838 |
| Product | PKG, BIPOLAR FORCEPS, MICRO TIP, 45CM, P/N 0250080115 nationwide in US and worldwide: Algeria, Argentina, Australia, Bolivia, Brazil, Canada, Chile, China, Colombia, Costa Rica, Ecuador, France, Germany, Greece, Guam, Guatemala, India, Italy, Japan, Jordan, Kuwait, Latin America, Malaysia, Mexico… |
| Product code | KOG |
| Recalling firm | Stryker Endoscopy |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 17, 2015 |
| FEI number | 2936485 |
At a glance
- None Linked 510(k)s
- 100–999 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