Device recall
Z-1112-2014: Oxoid Legionella BCYE Growth Supplement, For 500 ml of medium, SR0110C, packaged…
FDA device recall · Class II · Remel Inc
Key facts
| Recall number (Z-number) | Z-1112-2014 |
|---|---|
| Recall event | 67415 |
| Product | Oxoid Legionella BCYE Growth Supplement, For 500 ml of medium, SR0110C, packaged 10 vials/box, lyophilized. The firm name on the label is Oxoid Ltd., Basingstoke, Hants, England. The product is used for the isolation of Legionella species from clinical and environmental samples. When the product is… |
| Product code | JSK |
| Recalling firm | Remel Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 23, 2014 |
| 510(k) numbers | K831469 |
| FEI number | 1924669 |
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