Device recall
Z-1843-2016: AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd ST-9…
FDA device recall · Class II · Medscience Inc
Key facts
| Recall number (Z-number) | Z-1843-2016 |
|---|---|
| Recall event | 73664 |
| Product | AllergiEnd ST-9 Multiple Skin Test Applicator (Item 1000) and AllergiEnd ST-9 Multiple Well Test Tray (Item (1001). Contents: 8 applicators to perform up to 72 skin tests. Perform a multi-site skin test to identify reactions to certain allergens using a non-invasive applicator that contains 70… |
| Product code | LDH |
| Recalling firm | Medscience Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 13, 2017 |
| FEI number | 3010131789 |
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