Device recall
Z-2365-2015: Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209
FDA device recall · Class II · Cadence Inc.
Key facts
| Recall number (Z-number) | Z-2365-2015 |
|---|---|
| Recall event | 71674 |
| Product | Micro-Mate Tuberculin Glass Syringe, Non-sterile Catalog numbers 5208, 5209 |
| Product code | GAA |
| Recalling firm | Cadence Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 29, 2016 |
| FEI number | 1213649 |
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