Device recall
Z-2057-2016: dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal…
FDA device recall · Class II · Dynarex Corporation
Key facts
| Recall number (Z-number) | Z-2057-2016 |
|---|---|
| Recall event | 73584 |
| Product | dynarex Specimen Containers, Screw-On, Leak-Resistant Lid, Tamper-Evident Seal, Sterile, Single Use Only Product Usage:containers for sample collection |
| Product code | NNI |
| Recalling firm | Dynarex Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 6, 2018 |
| FEI number | 2431014 |
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