Device recall
Z-1996-2009: Coloplast, InterDry Ag 10" x 144" Roll P/N 6791001400, Manufactured for…
FDA device recall · Class III · Coloplast Corp Skin Care Div
Key facts
| Recall number (Z-number) | Z-1996-2009 |
|---|---|
| Recall event | 52801 |
| Product | Coloplast, InterDry Ag 10" x 144" Roll P/N 6791001400, Manufactured for Coloplast A/S DK-3050 Humlebaek, Denmark, Distributed by Coloplast Corp Minneapolis MN 55411. InterDry" is a non-sterile, knitted, polyurethane-coated polyester textile impregnated with an antimicrobial silver complex used for… |
| Product code | FRL |
| Recalling firm | Coloplast Corp Skin Care Div |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jan 11, 2011 |
| FEI number | 2125337 |
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