Device recall
Z-0902-2020: JAPAN CS ELITE FASTPACK, 225ML - Product Usage: its related accessory components…
FDA device recall · Class II · Haemonetics Corporation
Key facts
| Recall number (Z-number) | Z-0902-2020 |
|---|---|
| Recall event | 84183 |
| Product | JAPAN CS ELITE FASTPACK, 225ML - Product Usage: its related accessory components are intended for use to recover blood shed during or subsequent to an operation or as a result of trauma, processing the blood by a centrifugation and washing procedure, and pumping this processed red cell product to… |
| Product code | CAC |
| Recalling firm | Haemonetics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 6, 2020 |
| FEI number | 1219343 |
At a glance
- None Linked 510(k)s
- 10–99 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