Device recall
Z-1816-2010: Excyte Slider Barcode Tube Adapter used with Excyte Vacuum or Non-Vacuum ESR…
FDA device recall · Class III · Vital Diagnostics, Inc.
Key facts
| Recall number (Z-number) | Z-1816-2010 |
|---|---|
| Recall event | 55535 |
| Product | Excyte Slider Barcode Tube Adapter used with Excyte Vacuum or Non-Vacuum ESR Tubes. Single Use. Product Number: EX-I0552. Manufactured by Vital Diagnostics S.R.L., Italy. Slider allows a larger label to be applied to the ESR tube. |
| Product code | GHC |
| Recalling firm | Vital Diagnostics, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Sep 13, 2010 |
| FEI number | 1717966 |
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