Device recall
Z-0572-03: Ear Loop Procedure Masks, For one time use only, Glass-Free, Reorder No. 2201…
FDA device recall · Class II · Dynarex Corporation
Key facts
| Recall number (Z-number) | Z-0572-03 |
|---|---|
| Recall event | 25310 |
| Product | Ear Loop Procedure Masks, For one time use only, Glass-Free, Reorder No. 2201, packed in a cardboard box (unit box). Manufactured for dynarex Corporation, Brewster, NY 10509. Made in China. Product is labeled with a Latex-free symbol that states ''This product does not contain any natural rubber… |
| Product code | FXX |
| Recalling firm | Dynarex Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 30, 2012 |
| FEI number | 2431014 |
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