Device recall
Z-2215-2016: Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The…
FDA device recall · Class I · Draeger Medical, Inc.
Key facts
| Recall number (Z-number) | Z-2215-2016 |
|---|---|
| Recall event | 74469 |
| Product | Oxylog 3000, Disposable Pediatric Patient Circuit, Catalog Number: 5704964 The VentStar Oxylog 3000F disposable pediatric patient breathing circuit is used with the Drger Oxylog 3000 and Oxylog 3000 plus Emergency Transport Ventilators. |
| Product code | CBK |
| Recalling firm | Draeger Medical, Inc. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 14, 2018 |
| 510(k) numbers | K062267 |
| FEI number | 2517967 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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