Device recall
Z-0808-2013: Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged…
FDA device recall · Class II · Remel Inc
Key facts
| Recall number (Z-number) | Z-0808-2013 |
|---|---|
| Recall event | 63556 |
| Product | Oxoid Antimicrobial Susceptibility Discs, Cefoxitin 30ug REF CT0119B, packaged with 50 discs per cartridge, 5 cartridges per box. The responsible firm name on the label is Oxoid Ltd., Basingstoke, Hants, UK. |
| Product code | JTN |
| Recalling firm | Remel Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2013 |
| 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