Device recall
Z-2848-2011: Vital Signs- A GE Healthcare Company - Hygroscopic Condenser Humidifier…
FDA device recall · Class I · Vital Signs Devices, a GE Healthcare Company
Key facts
| Recall number (Z-number) | Z-2848-2011 |
|---|---|
| Recall event | 59047 |
| Product | Vital Signs- A GE Healthcare Company - Hygroscopic Condenser Humidifier (HCH)/Anesthesia Breathing Circuit; GE Medical Systems SCS 283 rue de la Miniere 78530 BUC, France p +33.1.30.70.40.40; Vital Signs Colorado Inc 11039 E. Lansing Circle Englewood, CO 80112 P +1.973.956.5300. The intended use of… |
| Product code | BYD |
| Recalling firm | Vital Signs Devices, a GE Healthcare Company |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Aug 6, 2014 |
| FEI number | 2242551 |
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