Device recall
Z-0613-03: REMEL CXM 30 Cefuroxime 30 mcg, Antimicrobial Susceptibility Test Disk, 50 disks…
FDA device recall · Class III · Remel, Inc.
Key facts
| Recall number (Z-number) | Z-0613-03 |
|---|---|
| Recall event | 25250 |
| Product | REMEL CXM 30 Cefuroxime 30 mcg, Antimicrobial Susceptibility Test Disk, 50 disks to a cartridge, 5 cartridges to a kit, catalog Number 33999. The label shows the product is ''Mfg for'' REMEL, Lenexa,KS. |
| Product code | JTN |
| Recalling firm | Remel, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 31, 2003 |
| FEI number | 1924669 |
At a glance
- None 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