Device recall
Z-1899-2011: 2380 MINI Hand-Held Tube Sealer Power Source (including a 23802000 Battery Pack)…
FDA device recall · Class II · Haemonetics Corporation
Key facts
| Recall number (Z-number) | Z-1899-2011 |
|---|---|
| Recall event | 57855 |
| Product | 2380 MINI Hand-Held Tube Sealer Power Source (including a 23802000 Battery Pack) The Model 2380 Power Source is an instrument that generates RF power for making seals on tubing made of RF reactive thermoplastic materials typically used in blood banks, blood processing facilities and transfusion… |
| Product code | KSD |
| Recalling firm | Haemonetics Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 6, 2012 |
| FEI number | 1219343 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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