Device recall
Z-2011-2009: Post Medical Valves VO870A-Y and VO870-A-Y-T PSI 2015, PSI 2015, CGA 870, Inlet…
FDA device recall · Class II · Intermed Gas Products Corporation
Key facts
| Recall number (Z-number) | Z-2011-2009 |
|---|---|
| Recall event | 51726 |
| Product | Post Medical Valves VO870A-Y and VO870-A-Y-T PSI 2015, PSI 2015, CGA 870, Inlet .750 STDS, Gas services (Oxygen), PSI 2015, Aluminum Cylinders, InterMed Gas Products LLC Industrial Division, 2056 Vista Parkway West Palm Beach, FL 33411. |
| Product code | ECX |
| Recalling firm | Intermed Gas Products Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 17, 2011 |
| FEI number | 3004485387 |
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