Device recall
Z-1258-03: ETHICON brand surgical device with an added label with the labeling Manufactured…
FDA device recall · Class II · International Surgical Supply, Inc.
Key facts
| Recall number (Z-number) | Z-1258-03 |
|---|---|
| Recall event | 27162 |
| Product | ETHICON brand surgical device with an added label with the labeling Manufactured by: MedSurg Solutions, 3025 Harbor Lane suite 104 Plymouth, MN 55447 and/or another additional label which states MEDSURG 3025 Harbor Lane, Suite 104, Plymouth, MN 55447 Steriliation Date:. The product labels also state… |
| Product code | KDC |
| Recalling firm | International Surgical Supply, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 6, 2012 |
| FEI number | 3003175501 |
At a glance
- None Linked 510(k)s
- 10–99 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