Device recall
Z-1796-2013: TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose…
FDA device recall · Class II · Haemonetics Corporation
Key facts
| Recall number (Z-number) | Z-1796-2013 |
|---|---|
| Recall event | 65635 |
| Product | TEG 5000 Thromboelastograph Coagulation Analyzer Product Usage: Multipurpose System for In Vitro Coagulation Studies |
| Product code | JPA |
| Recalling firm | Haemonetics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 4, 2015 |
| 510(k) numbers | K002177 |
| FEI number | 1219343 |
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