Device recall
Z-1815-2010: CaviBleach Wipes; a disinfectant medical device, active ingredient Sodium…
FDA device recall · Class II · Medtrol, Inc.
Key facts
| Recall number (Z-number) | Z-1815-2010 |
|---|---|
| Recall event | 55051 |
| Product | CaviBleach Wipes; a disinfectant medical device, active ingredient Sodium hypochlorite 0.525%; a single 9" x 9" towelette, pre-moistened with 0.525% - 0.656% sodium hypochlorite, packaged in a flexible poly foil pouch, 50 wipes per dispenser box, 8 boxes per case; Manufactured for Metrex Research… |
| Product code | LRJ |
| Recalling firm | Medtrol, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jun 23, 2010 |
| FEI number | 3002513493 |
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