Device recall
Z-2507-2015: KimVent* Wet Pak* Closed Suction System for Adults, 14 F, DSE, MDI (Product…
FDA device recall · Class II · Halyard Health, Inc
Key facts
| Recall number (Z-number) | Z-2507-2015 |
|---|---|
| Recall event | 71966 |
| Product | KimVent* Wet Pak* Closed Suction System for Adults, 14 F, DSE, MDI (Product 8224); KimVent* Wet Pak* Closed Suction System for Adults, 14 F, DSE (Product Code 22106); KimVent* Closed Suction System for Adults, 14 F, DSE, Wet Pak (Produce Code 221036) A tracheobronchial suction catheter is a device… |
| Product code | BSY |
| Recalling firm | Halyard Health, Inc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 12, 2016 |
| FEI number | 3011270181 |
At a glance
- None Linked 510(k)s
- 10–99 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