Device recall
Z-0132-2016: ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV…
FDA device recall · Class II · Baxter Healthcare Corp
Key facts
| Recall number (Z-number) | Z-0132-2016 |
|---|---|
| Recall event | 71260 |
| Product | ONE-LINK NON-DEHP Y-TYPE MICROBORE CATHETER EXTENSION SET NEEDLE-FREE IV CONNECTOR WITH NEUTRAL FLUID DISPLACEMENT |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 10, 2017 |
| 510(k) numbers | K132734 |
| FEI number | 1417572 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1,000+ 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