Device recall
Z-1846-2016: Reprocessed Microline Scissor Tips intended to be used with a reusable hand…
FDA device recall · Class II · STERILMED, INC.
Key facts
| Recall number (Z-number) | Z-1846-2016 |
|---|---|
| Recall event | 73871 |
| Product | Reprocessed Microline Scissor Tips intended to be used with a reusable hand piece and designed for minimally invasive and open surgical procedures to facilitate cutting, preparation, mobilization, and coagulation of tissue. Model #'s MIC3112, MIC3122, MIC3132, MIC3142, MIC3152, MIC3162. |
| Product code | NUJ |
| Recalling firm | STERILMED, INC. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 5, 2017 |
| 510(k) numbers | K073613 |
| FEI number | 3001237663 |
At a glance
- 1–9 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