Device recall
Z-1733-2009: Remel Middlebrook 7H10 Agar, Ref R01600, packaged 10 units/package. The firm…
FDA device recall · Class III · Remel, Inc
Key facts
| Recall number (Z-number) | Z-1733-2009 |
|---|---|
| Recall event | 52111 |
| Product | Remel Middlebrook 7H10 Agar, Ref R01600, packaged 10 units/package. The firm name on the label is Remel, Lenexa, KS. Solid Medium recommended for use in qualitative procedures for the isolation and cultivation of mycobacteria. |
| Product code | JSY |
| Recalling firm | Remel, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 15, 2009 |
| 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