Device recall
Z-1071-2007: NEFA Standard Solution Calibrator, Oleic Acid, 1 mmol/L, 4x10mL bottles per…
FDA device recall · Class III · Wako Chemicals USA, Inc.
Key facts
| Recall number (Z-number) | Z-1071-2007 |
|---|---|
| Recall event | 37921 |
| Product | NEFA Standard Solution Calibrator, Oleic Acid, 1 mmol/L, 4x10mL bottles per carton, Cat. 276-76491, labeled in part ***For in vitro diagnostic use ***Distributed by: Wako Chemicals, USA, Inc. 1600 Bellwood Road Richmond, VA 23237*** |
| Product code | JIT |
| Recalling firm | Wako Chemicals USA, Inc. |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 24, 2007 |
| FEI number | 3005625991 |
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