Device recall
Z-1724-2009: Amvex Integrated Flowmeter; a nonback-pressure compensated Bourdon gauge…
FDA device recall · Class II · Amvex Corporation
Key facts
| Recall number (Z-number) | Z-1724-2009 |
|---|---|
| Recall event | 52057 |
| Product | Amvex Integrated Flowmeter; a nonback-pressure compensated Bourdon gauge flowmeter; Amvex Corporation, 25B East Pearce St, Richmond Hill, Ontario L4B 2M9, Canada; Model No. FI. The Integrated Flowmeter has two parts, the Outlet port and the Flowmeter port. The Outlet port is intended to be used as a… |
| Product code | CCN |
| Recalling firm | Amvex Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 19, 2011 |
| FEI number | 3003272769 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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