Device recall
Z-0698-2016: WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of steam…
FDA device recall · Class II · Bigwall Enterprises
Key facts
| Recall number (Z-number) | Z-0698-2016 |
|---|---|
| Recall event | 72837 |
| Product | WARM STEAM Personal Steam Inhaler-Adjustable control to regulate flow of steam Soft touch facial & nasal masks" Product labeling reads in part: "Well at Walgreens***WARM Helps relieve symptoms of stuffy nasal passages, congestion or scratchy throats due to cold, flu or allergies |
| Product code | KFZ |
| Recalling firm | Bigwall Enterprises |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 6, 2018 |
| FEI number | 3008651658 |
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