Device recall
Z-0286-2020: Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood…
FDA device recall · Class III · Biomedical Polymers, Inc.
Key facts
| Recall number (Z-number) | Z-0286-2020 |
|---|---|
| Recall event | 83965 |
| Product | Hemo-Drop Blood Dispenser, Part Number BMP-HEMODROP, used for preparing blood samples. |
| Product code | LXG |
| Recalling firm | Biomedical Polymers, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 15, 2020 |
| FEI number | 1220502 |
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