Device recall
Z-2081-2013: Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat…
FDA device recall · Class III · Remel Inc
Key facts
| Recall number (Z-number) | Z-2081-2013 |
|---|---|
| Recall event | 64852 |
| Product | Oxoid Antimicrobial Susceptibility Test Discs F300 (Nitrofurantoin), Cat. #CT0036B, packaged in cartridges of 50 discs, 5 cartridges/pack. The firm name on the label is Oxoid Ltd., Basingstoke, Hampshire, England Product is used in the semi-quantitative agar diffusion test method for in-vitro… |
| Product code | JTN |
| Recalling firm | Remel Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jun 3, 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