Device recall
Z-0514-2013: Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient…
FDA device recall · Class I · Bunnell, Inc.
Key facts
| Recall number (Z-number) | Z-0514-2013 |
|---|---|
| Recall event | 63710 |
| Product | Patient Circuit used with the Life Pulse High Frequency Ventilator. The Patient Circuit is a required disposable component of the Life Pulse High Frequency Ventilator. Model #(s): Individual Patient Circuit - catalog # 902 Patient Circuit Kit - catalog # 937: contains 2 circuits and 2 x 2.5 & 2 x… |
| Product code | LSZ |
| Recalling firm | Bunnell, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 21, 2014 |
| PMA numbers | P850064 |
| FEI number | 3032745446 |
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