Device recall
Z-2235-2011: MicroStream Filterline Infant/Neonatal products: Part # 008598 - FILTERLINE H…
FDA device recall · Class I · Oridion Medical 1987 Ltd.
Key facts
| Recall number (Z-number) | Z-2235-2011 |
|---|---|
| Recall event | 58373 |
| Product | MicroStream Filterline Infant/Neonatal products: Part # 008598 - FILTERLINE H SET INF/NEO 25UN DRAEGER(Inf/Neo Airway Adapter). The adult/pediatric airway adapter and the adult/pediatric FilterLine and VitaLine sets are not affected by this recall. The intended use of Microstream Filter Lines is to… |
| Product code | CCK |
| Recalling firm | Oridion Medical 1987 Ltd. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Mar 19, 2012 |
| FEI number | 3001227743 |
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