Device recall
Z-0984-2022: Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100…
FDA device recall · Class III · Beckman Coulter, Inc.
Key facts
| Recall number (Z-number) | Z-0984-2022 |
|---|---|
| Recall event | 89655 |
| Product | Beckman Coulter IRISpec CA/CB/CC control, Catalog #800-7211, containing 3 x 100 mL bottles each of CA Control, CB Control, and CC Control. |
| Product code | JJW |
| Recalling firm | Beckman Coulter, Inc. |
| Recall class | Class III |
| Status | Open, Classified |
| FEI number | 3000203293 |
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