Device recall
Z-2068-2011: Advanced Instrument Model 2020 Multi-Sample Osmometer Intended to measure the…
FDA device recall · Class II · Advanced Instruments, Inc.
Key facts
| Recall number (Z-number) | Z-2068-2011 |
|---|---|
| Recall event | 58042 |
| Product | Advanced Instrument Model 2020 Multi-Sample Osmometer Intended to measure the osmotic pressure of body fluids. |
| Product code | GKE |
| Recalling firm | Advanced Instruments, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 1, 2011 |
| FEI number | 1217058 |
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