Device recall
Z-1434-2012: Clinical Chemistry Albumin BCG (AlbG) List Number 7D53-21 Clinical Chemistry…
FDA device recall · Class II · Abbott Laboratories Inc.
Key facts
| Recall number (Z-number) | Z-1434-2012 |
|---|---|
| Recall event | 55440 |
| Product | Clinical Chemistry Albumin BCG (AlbG) List Number 7D53-21 Clinical Chemistry Albumin BCG 510(k) K981758, Product Code CIX The Albumin BCG assay is used for the quantitation of albumin in human serum or plasma |
| Product code | CIX |
| Recalling firm | Abbott Laboratories Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 18, 2012 |
| 510(k) numbers | K981758 |
| FEI number | 2018433 |
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