Device recall
Z-0357-2007: Fibrin Analysis Catheter Testing System includes the component BD Vacutainer…
FDA device recall · Class II · Continental Medical Labs,Inc
Key facts
| Recall number (Z-number) | Z-0357-2007 |
|---|---|
| Recall event | 36655 |
| Product | Fibrin Analysis Catheter Testing System includes the component BD Vacutainer Luer-Lok Access Device; Catalogue #364902 as a finished sterile device, Non Pyrogenic in unopened undamaged package, Disposable/ Single use/ Do Not Reuse; for use with multi lumen; (4 Venous Catheter sizes) 20 cm. 12 fr… |
| Product code | GCJ |
| Recalling firm | Continental Medical Labs,Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 18, 2007 |
| FEI number | 2128604 |
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