Device recall
Z-1541-2012: Trima Accel Automated Blood Collection System, catalog number 917000000…
FDA device recall · Class II · CaridianBCT, Inc.
Key facts
| Recall number (Z-number) | Z-1541-2012 |
|---|---|
| Recall event | 53196 |
| Product | Trima Accel Automated Blood Collection System, catalog number 917000000, Caridian BCT, Lakewood, CO 80215 USA. Product Usage: Automated Blood Collection System for use in humans. |
| Product code | KZE |
| Recalling firm | CaridianBCT, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 25, 2012 |
| 510(k) numbers | K090003 |
| FEI number | 1000117351 |
At a glance
- 1–9 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