Device recall
Z-0528-2014: Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg…
FDA device recall · Class III · Remel Inc
Key facts
| Recall number (Z-number) | Z-0528-2014 |
|---|---|
| Recall event | 65734 |
| Product | Oxoid Antimicrobial Susceptibility Test Discs, CTO425B Ciprofloxacin CIP 5 mcg, 50 discs per cartridge, 5 cartridges per box. The firm name on the box label is Oxoid Ltd., Basingstoke, UK. Used in the semi-quantitative agar diffusion test method for in vitro susceptibility testing to assist in the… |
| Product code | JTN |
| Recalling firm | Remel Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 12, 2014 |
| 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