Device recall
Z-0722-2008: PML -- Vitek NH ID Card (NHI) Set - Quality Control kit for culture media. Each…
FDA device recall · Class III · PML, Inc. dba Pml Microbiologicals Inc.
Key facts
| Recall number (Z-number) | Z-0722-2008 |
|---|---|
| Recall event | 45530 |
| Product | PML -- Vitek NH ID Card (NHI) Set - Quality Control kit for culture media. Each kit includes a 5 pack of LyfoCults Haemophilus parainfluenzae - Lot # 185-1 Exp 13AUG2008. PML Micrcobiologicals, 27120 SW 95th Avenue, Wilsonville, Oregon 97070 |
| Product code | JTR |
| Recalling firm | PML, Inc. dba Pml Microbiologicals Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Apr 7, 2011 |
| FEI number | 3017344 |
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