Device recall
Z-1596-2013: Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation…
FDA device recall · Class II · Steris Corporation
Key facts
| Recall number (Z-number) | Z-1596-2013 |
|---|---|
| Recall event | 65138 |
| Product | Quick Connect QLC1677E, QRC1699E, QPC1721E and QFC1683E. STERIS Corporation, Mentor, OH 44060 QLC1677E, QRC1699E, QPC1721E and QFC1683E contain processing instructions, a Quick Reference Wall Chart and a flow unit. The flow unit consists of a Quick Reference Card, tubing, tethers and adapters for… |
| Product code | MED |
| Recalling firm | Steris Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 2, 2013 |
| 510(k) numbers | K113520 |
| 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