Device recall
Z-1361-2015: Double Swivel Connector with Suction Port Connector, Airway (Extension) King…
FDA device recall · Class II · King Systems Corp.
Key facts
| Recall number (Z-number) | Z-1361-2015 |
|---|---|
| Recall event | 70610 |
| Product | Double Swivel Connector with Suction Port Connector, Airway (Extension) King Systems part 7169 Product Usage: An airway connector is a device intended to connect a breathing gas source to a tracheal tube, tracheostomy tube, or gas mask. The double swivel connector with suction port is an optional… |
| Product code | BZA |
| Recalling firm | King Systems Corp. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 27, 2015 |
| FEI number | 1824226 |
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