Device recall
Z-0803-2012: Salter Labs Bubble humidifier, with 6 PSI safety valve, 350cc, Latex Free…
FDA device recall · Class I · SALTER LABS
Key facts
| Recall number (Z-number) | Z-0803-2012 |
|---|---|
| Recall event | 60270 |
| Product | Salter Labs Bubble humidifier, with 6 PSI safety valve, 350cc, Latex Free; Single Patient use; used with supplemental oxygen therapy. Model Numbers 7600-0-50, E7600-0-50, NP7600-0-50 and special order patient kits that contain 7600 humidifiers. Patient kits have brand names of Salter Labs, AdvaCare… |
| Product code | BBT |
| Recalling firm | SALTER LABS |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Feb 15, 2012 |
| FEI number | 1314417 |
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