Device recall
Z-2732-2014: LAP-BAND AP SYSTEM AP Large with Access Port, Allergan, LAP-BAND AP SYSTEM…
FDA device recall · Class II · Apollo Endosurgery Inc
Key facts
| Recall number (Z-number) | Z-2732-2014 |
|---|---|
| Recall event | 69132 |
| Product | LAP-BAND AP SYSTEM AP Large with Access Port, Allergan, LAP-BAND AP SYSTEM Access Port I. Product was distributed for both the AP Large and AP Standard sizes. The LAP-BAND System is indicated for weight reduction for patients with obesity, with a Body Mass Index (BMI) of at least 40 kg/m2 or a BMI… |
| Product code | LTI |
| Recalling firm | Apollo Endosurgery Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 1, 2016 |
| 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