Device recall
Z-2714-2014: Hudson RCI Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only…
FDA device recall · Class I · Teleflex Medical
Key facts
| Recall number (Z-number) | Z-2714-2014 |
|---|---|
| Recall event | 69194 |
| Product | Hudson RCI Pediatric Anesthesia Breathing Circuits, Single Patient Use, Rx Only, Product Usage: To administer medical gases to a patient during anesthesia. It provides both an inhalation and exhalation route and may include a connector, adaptor, and Ypiece. |
| Product code | CAI |
| Recalling firm | Teleflex Medical |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 16, 2016 |
| FEI number | 3005747797 |
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