Device recall
Z-2296-2010: V. Mueller Peanut Sponges, Catalog number 23275-470, Sterile, For Single Use…
FDA device recall · Class II · He, Inc
Key facts
| Recall number (Z-number) | Z-2296-2010 |
|---|---|
| Recall event | 56420 |
| Product | V. Mueller Peanut Sponges, Catalog number 23275-470, Sterile, For Single Use Only, Size: 3/8, X-Ray Detectable In Holders, Distributed by Cardinal Health, McGaw Park, IL 60085 USA. There are various uses including as gauze/sponge internal, x-ray detectable and as dissectors. |
| Product code | GDI |
| Recalling firm | He, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 2, 2011 |
| FEI number | 1000112023 |
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