Device recall
Z-0621-2013: Fisher & Paykel Healthcare reusable breathing circuit. Non-heated breathing…
FDA device recall · Class I · Fisher & Paykel Healthcare, Ltd.
Key facts
| Recall number (Z-number) | Z-0621-2013 |
|---|---|
| Recall event | 63794 |
| Product | Fisher & Paykel Healthcare reusable breathing circuit. Non-heated breathing circuit, 1.8m or 6 feet in length. Oxygen therapy delivery system for adult patient. |
| Product code | BZO |
| Recalling firm | Fisher & Paykel Healthcare, Ltd. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jul 11, 2013 |
| FEI number | 3002806988 |
At a glance
- None 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