Device recall
Z-0765-04: QPC1680 Quick Connect, for Pentax 30/40/K Series Two-Channel GI Endoscopes, in…
FDA device recall · Class II · Steris Corp
Key facts
| Recall number (Z-number) | Z-0765-04 |
|---|---|
| Recall event | 28569 |
| Product | QPC1680 Quick Connect, for Pentax 30/40/K Series Two-Channel GI Endoscopes, in the Steris System 1 Sterile Processing System with the C1160 Universal Flexible Processing Tray, Cat No. QPT1680 |
| Product code | MED |
| Recalling firm | Steris Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 18, 2004 |
| 510(k) numbers | K875280 |
| FEI number | 1527821 |
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