Device recall
Z-0985-2010: Chlamydia Pneumoniae IgG ELISA 96 Well Kit, Catalog Number: CP083G The products…
FDA device recall · Class II · Calbiotech Inc
Key facts
| Recall number (Z-number) | Z-0985-2010 |
|---|---|
| Recall event | 50691 |
| Product | Chlamydia Pneumoniae IgG ELISA 96 Well Kit, Catalog Number: CP083G The products in question are all Enzyme Linked Immunosorbent Assay (ELISA) Test kits designed and marketed for Research Use Only. |
| Product code | LJC |
| Recalling firm | Calbiotech Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 5, 2010 |
| FEI number | 3002346973 |
At a glance
- None Linked 510(k)s
- 10–99 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