Device recall
Z-1184-2026: PREGNANCY TEST 24CT
FDA device recall · Class II · GOLD STAR DISTRIBUTION INC
Key facts
| Recall number (Z-number) | Z-1184-2026 |
|---|---|
| Recall event | 98234 |
| Product | PREGNANCY TEST 24CT |
| Product code | LCX |
| Recalling firm | GOLD STAR DISTRIBUTION INC |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3004388746 |
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