Device recall
Z-2856-2011: PALL Medical LeukoGuard LGB Arterial Line Leukocyte Reduction Filter with Bypass…
FDA device recall · Class II · Pall Corporation
Key facts
| Recall number (Z-number) | Z-2856-2011 |
|---|---|
| Recall event | 59259 |
| Product | PALL Medical LeukoGuard LGB Arterial Line Leukocyte Reduction Filter with Bypass Loop, STERILE. CATALOG/MODEL/Reorder Number: LGB. CLASSIFICATION NAME: Filter, Blood, Cardiopulmonary Bypass Arterial Line. COMMON/USUAL NAME: Arterial Line Filter with Bypass Loop. -- Manufactured by: PALL NEWQUAY… |
| Product code | LGB |
| Recalling firm | Pall Corporation |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 3, 2012 |
| 510(k) numbers | K902518 |
| FEI number | 2432733 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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