Device recall
Z-2117-2014: CPR Shield With One Way Valve and Barrier Filter, Reorder No. 4921 --- Dynarex…
FDA device recall · Class II · Dynarex Corporation
Key facts
| Recall number (Z-number) | Z-2117-2014 |
|---|---|
| Recall event | 68681 |
| Product | CPR Shield With One Way Valve and Barrier Filter, Reorder No. 4921 --- Dynarex label, 100 per case --- Manufactured for: Dynarex Corporation - Made in China. Used as a physical barrier for mouth to mouth resuscitation. |
| Product code | CBP |
| Recalling firm | Dynarex Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 20, 2017 |
| 510(k) numbers | K052743 |
| FEI number | 2431014 |
At a glance
- 1–9 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