Device recall
Z-2462-2008: Quick Connect component p/n 201048. The component is contained in QPC1713 and…
FDA device recall · Class II · Steris Corp
Key facts
| Recall number (Z-number) | Z-2462-2008 |
|---|---|
| Recall event | 49390 |
| Product | Quick Connect component p/n 201048. The component is contained in QPC1713 and QPC1724 Quick Connects. The QPC1724 is used to attach Pentax 70/70K/72/72K/80K/81K/90i/90K SERIES GI ENDOSCOPES WITH WATER JET to the C1160 Universal Flexible Processing Tray in the SYSTEM 1 Sterile Processing System. The… |
| Product code | MED |
| Recalling firm | Steris Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 26, 2013 |
| 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