Device recall
Z-0988-2011: Southmedic/Personna Safety Scalpel with Personna Plus Blades, Reorder No…
FDA device recall · Class II · Southmedic, Inc.
Key facts
| Recall number (Z-number) | Z-0988-2011 |
|---|---|
| Recall event | 56963 |
| Product | Southmedic/Personna Safety Scalpel with Personna Plus Blades, Reorder No. 73-0610, Size #10, General Surgical Use, Sterile, unless package is damaged or opened., Southmedic Inc., 50 Alliance Blvd., Barrie, ON., Canada L4M 5K3 www.southmedic.com, Made in Canada. |
| Product code | GDX |
| Recalling firm | Southmedic, Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 18, 2011 |
| FEI number | 3001717360 |
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