Device recall
Z-1858-2012: Hartmann Sterilux Ref 56910000 Sterile Premium gauze sponge 4"x4" 12-ply 24…
FDA device recall · Class II · Hartmann USA, Inc
Key facts
| Recall number (Z-number) | Z-1858-2012 |
|---|---|
| Recall event | 61899 |
| Product | Hartmann Sterilux Ref 56910000 Sterile Premium gauze sponge 4"x4" 12-ply 24 boxes/case 1200 total sponges For use in wound cleansing, debriding of wounds, wound packing, covering and swabbing |
| Product code | NAB |
| Recalling firm | Hartmann USA, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2014 |
| FEI number | 1218946 |
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