Device recall
Z-0635-03: Latex examination gloves, Uniseal brand.
FDA device recall · Class II · American Healthcare Products Inc
Key facts
| Recall number (Z-number) | Z-0635-03 |
|---|---|
| Recall event | 25611 |
| Product | Latex examination gloves, Uniseal brand. |
| Product code | LYY |
| Recalling firm | American Healthcare Products Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 24, 2005 |
| 510(k) numbers | K945164 |
| FEI number | 1000099913 |
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