Device recall
Z-2613-2014: ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber…
FDA device recall · Class II · Baxter Healthcare Corp
Key facts
| Recall number (Z-number) | Z-2613-2014 |
|---|---|
| Recall event | 68843 |
| Product | ***Baxter***Buretrol Solution Set***105" (2.7 m)***150 mL Burette***Drip Chamber Filter Valve***3 Injection Sites Male Luer Lock Adapter with***Retractable Collar***Fluid path is Sterile, Nonpyrogenic***Indications for Use: For the administration of fluids from a container into the patient's… |
| Product code | FPA |
| Recalling firm | Baxter Healthcare Corp |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Mar 15, 2016 |
| 510(k) numbers | K123874 |
| 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