Device recall
Z-1190-2019: BIOPHEN LMWH Control C4, REF 224201
FDA device recall · Class III · Aniara Diagnostica LLC
Key facts
| Recall number (Z-number) | Z-1190-2019 |
|---|---|
| Recall event | 82468 |
| Product | BIOPHEN LMWH Control C4, REF 224201 |
| Product code | GGN |
| Recalling firm | Aniara Diagnostica LLC |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 12, 2019 |
| 510(k) numbers | K051472 |
| FEI number | 3005017664 |
At a glance
- 1–9 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