Device recall
Z-1050-2019: LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-4RT3 Rev B Product Usage: used…
FDA device recall · Class II · LW Scientific, Inc.
Key facts
| Recall number (Z-number) | Z-1050-2019 |
|---|---|
| Recall event | 82214 |
| Product | LW Scientific ZIP IQ Combo Centrifuge, ZIC-CMBO-4RT3 Rev B Product Usage: used as a general purpose centrifuge to spin down blood in hematocrit tubes with additional rotors to spin other fluids in test tubes (15ml and 50ml), microtubes, and PCR strips |
| Product code | JQC |
| Recalling firm | LW Scientific, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 7, 2021 |
| FEI number | 3000251573 |
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