Device recall
Z-2272-2013: Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia breathing…
FDA device recall · Class I · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-2272-2013 |
|---|---|
| Recall event | 66184 |
| Product | Universal Flex2 Breathing Circuit Class I 510(k) Exempt An anesthesia breathing circuit is a device that is intended to administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Y-piece. |
| Product code | CAI |
| Recalling firm | King Systems Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Nov 18, 2013 |
| FEI number | 1824226 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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