Device recall
Z-0443-2016: Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10), REF# CT0024B…
FDA device recall · Class II · Remel Inc
Key facts
| Recall number (Z-number) | Z-0443-2016 |
|---|---|
| Recall event | 72525 |
| Product | Oxoid Gentamicin Antimicrobial Susceptibility Testing Disc (CN10), REF# CT0024B packaged in packs of 5 cartridges - 50 disc/cartridge. Used in the semi-quantitative agar diffusion test method for in vitro susceptibility testing to assist in the determination of a suitable antibiotic agent for… |
| Product code | JTN |
| Recalling firm | Remel Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 13, 2017 |
| 510(k) numbers | K860153 |
| FEI number | 1924669 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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