Device recall
Z-0174-2019: Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061
FDA device recall · Class II · Life Technologies, Corp.
Key facts
| Recall number (Z-number) | Z-0174-2019 |
|---|---|
| Recall event | 81052 |
| Product | Gibco GlutaMAX Supplement, for In-Vitro Diagnostic Use SKU 35050061 |
| Product code | KIT |
| Recalling firm | Life Technologies, Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 29, 2020 |
| FEI number | 1317268 |
At a glance
- None 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