Device recall
Z-0014-2013: Baxter Clearlink System Buretrol Solution Set, 115" (2.9 m) with 150 mL…
FDA device recall · Class I · Baxter Healthcare Corp.
Key facts
| Recall number (Z-number) | Z-0014-2013 |
|---|---|
| Recall event | 63059 |
| Product | Baxter Clearlink System Buretrol Solution Set, 115" (2.9 m) with 150 mL Clearlink Burette (Ball-Valve Drip Chamber); a sterile Rx IV fluid pathway device. Product Usage: The device is used for the administration of fluids from a container into the patient's vascular system through a vascular access… |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp. |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Dec 29, 2017 |
| 510(k) numbers | K984381 |
| FEI number | 1416980 |
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