Device recall
Z-1079-2013: CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381…
FDA device recall · Class II · Thermo Fisher Scientific (Asheville) LLC
Key facts
| Recall number (Z-number) | Z-1079-2013 |
|---|---|
| Recall event | 64418 |
| Product | CO2 Incubators (General Purpose Incubator), model numbers 370, 371, 380, 381, 3307, 3308, 3310, 3311, 3540, 3541, 3542, 3543, 3584, 3585, 3598, and 3599. Product Usage: Incubators are designed to maintain an optimal environment for the incubation of tissue and cell samples. These models are designed… |
| Product code | JTQ |
| Recalling firm | Thermo Fisher Scientific (Asheville) LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Apr 14, 2015 |
| FEI number | 1523845 |
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