Device recall
Z-0268-2007: Medline Premium Wet Skin Prep Tray, Sterile, Latex Free; a single use surgical…
FDA device recall · Class II · Medline Industries Inc
Key facts
| Recall number (Z-number) | Z-0268-2007 |
|---|---|
| Recall event | 36919 |
| Product | Medline Premium Wet Skin Prep Tray, Sterile, Latex Free; a single use surgical convenience tray, EO sterilized; Reorder DYND70660; 20 trays per case; Medline Industries, Inc., Mundelein, IL 60060-4486 |
| Product code | LRO |
| Recalling firm | Medline Industries Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 31, 2008 |
| 510(k) numbers | K914174 |
| FEI number | 1417592 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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