Device recall
Z-0322-06: OLA 2500 Olympus Lab Automation Systems to include the following models (all…
FDA device recall · Class III · Olympus America, Inc
Key facts
| Recall number (Z-number) | Z-0322-06 |
|---|---|
| Recall event | 34058 |
| Product | OLA 2500 Olympus Lab Automation Systems to include the following models (all serial numbers): S2 Full Size, S3 Full Size, Standard Full Size and High Speed Full Size (Aliquoter) manufactured by Olympus Life and Material Science Europa GmbH, Germany and distributed by Olympus America, Inc., 3131 W… |
| Product code | JQP |
| Recalling firm | Olympus America, Inc |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 10, 2008 |
| FEI number | 3002406108 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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