Device recall
Z-2145-2014: Instructions for Use for the blue endo MOREsolution Electromechanical…
FDA device recall · Class II · Market-Tiers Inc
Key facts
| Recall number (Z-number) | Z-2145-2014 |
|---|---|
| Recall event | 68745 |
| Product | Instructions for Use for the blue endo MOREsolution Electromechanical Laparoscopic Morcellator System, Model 55-000011, consisting of the control unit, hand-grip, flexible shaft, trocars/obturators, sleeves, valves, and blades. |
| Product code | HET |
| Recalling firm | Market-Tiers Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 11, 2015 |
| 510(k) numbers | K091010 |
| FEI number | 1000219003 |
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