Device recall
Z-0208-2013: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model…
FDA device recall · Class II · Sechrist Industries Inc
Key facts
| Recall number (Z-number) | Z-0208-2013 |
|---|---|
| Recall event | 52796 |
| Product | Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model 3300E/ER The Hyperbaric Chamber is intended to provide 100% oxygen to the patient at greater than ambient pressures. |
| Product code | CBF |
| Recalling firm | Sechrist Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 6, 2012 |
| 510(k) numbers | K052713 |
| FEI number | 2020676 |
At a glance
- 1–9 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