Device recall
Z-0967-2007: Steris QFC1728 and QFC1729 Quick Connects used in connections and processing…
FDA device recall · Class II · Steris Corp
Key facts
| Recall number (Z-number) | Z-0967-2007 |
|---|---|
| Recall event | 37493 |
| Product | Steris QFC1728 and QFC1729 Quick Connects used in connections and processing endoscopes. The QFC1728 is used to process the Fujinon 250/270/450/470/490 Group 5 and 530/590 series GI Endoscopes w/o Water Jet. The QFC1729 is used to process 250/450 Group 5 and 530/590 series Endoscopes w/ Water Jet. |
| Product code | MED |
| Recalling firm | Steris Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 1, 2012 |
| 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