Device recall
Z-0513-2019: PerkinElmer QSight 210 MD Mass Spectrometer Simplicity 3Q MD v1.0 with Hot Fix 2…
FDA device recall · Class II · PerkinElmer Health Sciences Canada, Inc.
Key facts
| Recall number (Z-number) | Z-0513-2019 |
|---|---|
| Recall event | 81266 |
| Product | PerkinElmer QSight 210 MD Mass Spectrometer Simplicity 3Q MD v1.0 with Hot Fix 2 Software intended to identify compounds in human samples by ionizing the compound and separating the resulting ions. Part Number: BC004872 |
| Product code | DOP |
| Recalling firm | PerkinElmer Health Sciences Canada, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 17, 2019 |
| FEI number | 3013944243 |
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