Device recall
Z-0323-06: 0.10% BreathScan Alcohol Detector manufactured for WNCK, Inc., The Woodlands, TX…
FDA device recall · Class II · WNCK, Inc
Key facts
| Recall number (Z-number) | Z-0323-06 |
|---|---|
| Recall event | 34090 |
| Product | 0.10% BreathScan Alcohol Detector manufactured for WNCK, Inc., The Woodlands, TX by Howard Industries, Inc., Columbus, OH (crystals) and James Alexander Corp., Blairstown, NJ (general device assembly). Product sold in bulk and individually packaged. Bulk product (500-1000 units) distributed in… |
| Product code | DJZ |
| Recalling firm | WNCK, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 25, 2007 |
| FEI number | 3004057121 |
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