Device recall
Z-0418-2011: LAP-BAND Adjustable Gastric Band System; Product codes: B-2105 (ACCSS PRT II KIT…
FDA device recall · Class II · Allergan
Key facts
| Recall number (Z-number) | Z-0418-2011 |
|---|---|
| Recall event | 57094 |
| Product | LAP-BAND Adjustable Gastric Band System; Product codes: B-2105 (ACCSS PRT II KIT (0-10CC) US), B-2106 (ACCESS PRT II KIT (0-14CC) US), B-2210 (LP-BND SYS, 9.75, STER, US), B-2215 (LAP-BAND 9.75 W/ACC PRT II US), B-2220 (LP-BND SYS, 10.0, STER, US), B-2225 (LAP-BND 10.0,ACCESS PORT II,US), B-2255… |
| Product code | LTI |
| Recalling firm | Allergan |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 22, 2010 |
| PMA numbers | P000008 |
| FEI number | 2024601 |
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