Device recall
Z-1812-2009: Remel BactiSwab NPG Collection and Transport System, Sterile, 100 swab…
FDA device recall · Class III · Remel, Inc
Key facts
| Recall number (Z-number) | Z-1812-2009 |
|---|---|
| Recall event | 52160 |
| Product | Remel BactiSwab NPG Collection and Transport System, Sterile, 100 swab units/box, Catalog 12300. The firm name on the label is Remel, Lenexa, KS. Collection and transportation of clinical specimens to the laboratory for microbiological examination when swab collection is appropriate. |
| Product code | LIO |
| Recalling firm | Remel, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 15, 2010 |
| 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