Device recall
Z-1995-2016: Flexichamber Anti-Static Valved Collapsible Holding Chamber, used by patients to…
FDA device recall · Class II · FSC Laboratories, Inc
Key facts
| Recall number (Z-number) | Z-1995-2016 |
|---|---|
| Recall event | 74197 |
| Product | Flexichamber Anti-Static Valved Collapsible Holding Chamber, used by patients to administer aerosolized medication from most pressurized Metered Dose Inhalers(pMDIs). |
| Product code | NVP |
| Recalling firm | FSC Laboratories, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 10, 2017 |
| 510(k) numbers | K140062 |
| FEI number | 3008832322 |
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