Device recall
Z-0413-2011: Detachol adhesive remover, 4 fl oz (118 mL), Marketed by Eloquest Healthcare…
FDA device recall · Class III · Ferndale Laboratories, Inc.
Key facts
| Recall number (Z-number) | Z-0413-2011 |
|---|---|
| Recall event | 56580 |
| Product | Detachol adhesive remover, 4 fl oz (118 mL), Marketed by Eloquest Healthcare, Inc., a Ferndale Pharma Group company, Manufactured by Ferndale Laboratories, Inc., Ferndale, MI 48220 U.S.A. |
| Product code | KOX |
| Recalling firm | Ferndale Laboratories, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 2, 2011 |
| FEI number | 1811212 |
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