Device recall
Z-1402-2017: CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is…
FDA device recall · Class II · Metrex Research, LLC.
Key facts
| Recall number (Z-number) | Z-1402-2017 |
|---|---|
| Recall event | 76318 |
| Product | CaviWipes1 Extra Large, Part No. 13-5150 The brand name of the device is CaviWipes1 Extra Large, a surface disinfectant. The device has been assigned the product code LRJ (General Purpose Disinfectant) by the FDA and is classified as a Class I Medical Device. CaviWipes1 Extra Large is intended to be… |
| Product code | LRJ |
| Recalling firm | Metrex Research, LLC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 1, 2017 |
| FEI number | 1000117344 |
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