Device recall
Z-0078-2011: EasyRA Cuvette Segment 1, P/N 007000-001 (In Vitro Diagnostic) EasyRA Cuvette…
FDA device recall · Class II · Medica Corporation
Key facts
| Recall number (Z-number) | Z-0078-2011 |
|---|---|
| Recall event | 55150 |
| Product | EasyRA Cuvette Segment 1, P/N 007000-001 (In Vitro Diagnostic ) EasyRA Cuvette Segments included in the following Kits: EasyRA Cuvettes, REF 10700-4 Startup Kit - Chemistry, REF 10990 Startup Kit - Chemistry & ISE, REF 10991 |
| Product code | JJE |
| Recalling firm | Medica Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 7, 2011 |
| 510(k) numbers | K070057, K072249 |
| FEI number | 1220972 |
At a glance
- 1–9 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