Device recall
Z-0694-2012: MERZ AESTHETICS, 27G X 1.0 " (25MM) Cannula, Sterile R, QTY 20, Model 9015M1X20…
FDA device recall · Class III · Merz Aesthetics, Inc.
Key facts
| Recall number (Z-number) | Z-0694-2012 |
|---|---|
| Recall event | 60851 |
| Product | MERZ AESTHETICS, 27G X 1.0 " (25MM) Cannula, Sterile R, QTY 20, Model 9015M1X20, Distributed by Merz Aesthetics, In., Manufactured by TSK Laboratory. The intended use of the Cannula is the injection of fluids into, or withdrawal of fluids from, parts of the body below the surface of the skin. |
| Product code | FMI |
| Recalling firm | Merz Aesthetics, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 27, 2012 |
| 510(k) numbers | K970370 |
| FEI number | 3003407669 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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