Device recall
Z-2743-2018: Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band…
FDA device recall · Class II · Apollo Endosurgery Inc
Key facts
| Recall number (Z-number) | Z-2743-2018 |
|---|---|
| Recall event | 80079 |
| Product | Apollo Lap-Band AP System Small with RapidPort EZ Product Usage: The Lap-Band system consists of a silicone band with pillows that are filled with saline and a buckle that joins the ends of the bands together, an access port and silicone tubing that connects the band to the access port. The band is… |
| Product code | LTI |
| Recalling firm | Apollo Endosurgery Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 6, 2020 |
| PMA numbers | P000008 |
| FEI number | 3006722112 |
At a glance
- None 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