Device recall
Z-0215-2008: Matrix MAX3 Actuator, Catalog Number: MAX30 A300545A252L0V000, SKF USA, Inc…
FDA device recall · Class II · Skf USA Inc
Key facts
| Recall number (Z-number) | Z-0215-2008 |
|---|---|
| Recall event | 44962 |
| Product | Matrix MAX3 Actuator, Catalog Number : MAX30 A300545A252L0V000, SKF USA, Inc. Norristown, PA 19403 |
| Recalling firm | Skf USA Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 26, 2013 |
| FEI number | 3003668692 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
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