Device recall
Z-2365-2016: Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed one per…
FDA device recall · Class II · Invacare Corporation
Key facts
| Recall number (Z-number) | Z-2365-2016 |
|---|---|
| Recall event | 74581 |
| Product | Invacare Precise Rx Pediatric Flowmeter Model Number: IRCPF16 AW. Packed one per carton. The lnvacare Precise Rx" Pediatric Flowmeter adapts to lnvacare Concentrators for low-flow usage.The gauge has a scale printed on the front side and the back side. The front scale is the primary source for… |
| Product code | NFB |
| Recalling firm | Invacare Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 7, 2017 |
| 510(k) numbers | K914488 |
| FEI number | 3002889431 |
At a glance
- 1–9 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