Device recall
Z-0790-03: Vicks brand Warm Mist Humidifier, Model V610, ''Pure Warm Moisturizer for…
FDA device recall · Class II · KAZ Inc.
Key facts
| Recall number (Z-number) | Z-0790-03 |
|---|---|
| Recall event | 26000 |
| Product | Vicks brand Warm Mist Humidifier, Model V610, ''Pure Warm Moisturizer for Soothing Relief of Cold and Flu Symptoms'' sold over the counter. Firm on the label: Distributed by Kaz Inc., under license from the Procter & Gamble Company, Cincinnati, OH 45202. UPC code 3 28785 20610 4. |
| Product code | KFZ |
| Recalling firm | KAZ Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2005 |
| FEI number | 1314800 |
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