Device recall
Z-2096-2013: OLA Buffer For Laboratory Use; Contents: 1 tube with buffered solution…
FDA device recall · Class III · Celera Corporation
Key facts
| Recall number (Z-number) | Z-2096-2013 |
|---|---|
| Recall event | 65874 |
| Product | OLA Buffer For Laboratory Use; Contents: 1 tube with buffered solution containing MgCl2 (80 M) and KCL (300 M. 10.0ml.) PN: 50003300; Store at d - 15C. Product Usage: General Purpose Reagent for laboratory use. |
| Product code | LDT |
| Recalling firm | Celera Corporation |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Oct 1, 2013 |
| FEI number | 3004008801 |
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