Device recall
Z-1865-2017: Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory…
FDA device recall · Class II · Avid Medical, Inc.
Key facts
| Recall number (Z-number) | Z-1865-2017 |
|---|---|
| Recall event | 76745 |
| Product | Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory hematology studies including but not limited to lead level testing, FEP level testing, and CBC testing. |
| Product code | OKV |
| Recalling firm | Avid Medical, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 7, 2017 |
| FEI number | 1047429 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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