Device recall
Z-0487-03: Ultrakleen KSponge II Spears Catalog #: K20-5012
FDA device recall · Class II · Ultracell Medical Technologies
Key facts
| Recall number (Z-number) | Z-0487-03 |
|---|---|
| Recall event | 25224 |
| Product | Ultrakleen KSponge II Spears Catalog #: K20-5012 |
| Product code | HOZ |
| Recalling firm | Ultracell Medical Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 1, 2012 |
| 510(k) numbers | K923922 |
| FEI number | 1000120594 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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