Device recall
Z-1423-2012: Non-sterile wound closure strips, packaged as follows: DeRoyal NS EPISEAL, Wound…
FDA device recall · Class III · Deroyal Industries, Inc. Lafollette
Key facts
| Recall number (Z-number) | Z-1423-2012 |
|---|---|
| Recall event | 61403 |
| Product | Non-sterile wound closure strips, packaged as follows: DeRoyal NS EPISEAL, Wound Closure Strips, REF 46-202N, Distributed by: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849; Manufacturer: DeRoyal Industries, 200 DeBusk Lane, Powell TN 37849 DeRoyal NS EPISEAL, Wound Closure Strips, REF… |
| Product code | KGX |
| Recalling firm | Deroyal Industries, Inc. Lafollette |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 10, 2013 |
| FEI number | 3005011024 |
At a glance
- None Linked 510(k)s
- 1–9 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