Device recall
Z-1910-2025: ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample)
FDA device recall · Class II · Healthmark Industries Co., Inc.
Key facts
| Recall number (Z-number) | Z-1910-2025 |
|---|---|
| Recall event | 96823 |
| Product | ChannelCheck Convenience Pack, Model Numbers UCC-222CP and UCC-222-ESP (Sample) |
| Product code | MNL |
| Recalling firm | Healthmark Industries Co., Inc. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1000160387 |
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