Device recall
Z-0728-2018: JANUS & JANUS G3 Automated Workstation is an automated programmable liquid…
FDA device recall · Class III · Perkinelmer Life Sciences, Inc.
Key facts
| Recall number (Z-number) | Z-0728-2018 |
|---|---|
| Recall event | 79015 |
| Product | JANUS & JANUS G3 Automated Workstation is an automated programmable liquid handling instrument intended for use in clinical settings to facilitate the pipetting and dilution of solutions in sample preparation work flows. |
| Product code | JQW |
| Recalling firm | Perkinelmer Life Sciences, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 31, 2018 |
| FEI number | 1000513616 |
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