Device recall
Z-1400-2017: Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm…
FDA device recall · Class II · Remel Inc
Key facts
| Recall number (Z-number) | Z-1400-2017 |
|---|---|
| Recall event | 76445 |
| Product | Remel, Haemophilus Test Medium (Agar) in A) 100 mm REF R01503, and B) 150 mm plates REF R04033, |
| Product code | LKA |
| Recalling firm | Remel Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2019 |
| FEI number | 1924669 |
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