Device recall
Z-1043-2009: BEC Growth Chek Microbial Suspension - Candida albicans CA1 (100 dose), Product…
FDA device recall · Class III · Lexamed
Key facts
| Recall number (Z-number) | Z-1043-2009 |
|---|---|
| Recall event | 50821 |
| Product | BEC Growth Chek Microbial Suspension - Candida albicans CA1 (100 dose), Product #10231-100 Liquid suspensions used for performing USP Growth Promotion and Bacteriostasis/Fungistasis testing and other quality control measures for growth media. Certified to deliver less than 100 organisms per dose. |
| Product code | LRF |
| Recalling firm | Lexamed |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 9, 2009 |
| 510(k) numbers | K842579 |
| FEI number | 1525897 |
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