Device recall
Z-2123-2011: Lap-Band Access Port Needle 10-Pack, 20 G x 51 mm (2 in.), Product Code…
FDA device recall · Class II · Allergan
Key facts
| Recall number (Z-number) | Z-2123-2011 |
|---|---|
| Recall event | 58574 |
| Product | Lap-Band Access Port Needle 10-Pack, 20 G x 51 mm (2 in.), Product Code: 8-20302-10, Lot Number: 9L01N 20 gauge, 51 mm (2 in.) length non-coring deflected tip (Huber) needle, used with the LAP-BAND System for band adjustment. |
| Product code | LTI |
| Recalling firm | Allergan |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 6, 2012 |
| 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