Device recall
Z-0792-2013: Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and…
FDA device recall · Class III · Diagnostic Hybrids Inc
Key facts
| Recall number (Z-number) | Z-0792-2013 |
|---|---|
| Recall event | 64115 |
| Product | Diagnostic Hybrids, Inc., RhMK, Model #:49-0600, 49-0600A, 49-0102A, and 49-T075A. Culture media, used in the cultivation and amplification of viruses, such as respiratory viruses, enteroviruses, measles, and poliovirus from patient specimens. |
| Product code | LKA |
| Recalling firm | Diagnostic Hybrids Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 5, 2013 |
| FEI number | 1000122536 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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