Device recall
Z-0139-06: Spanish Patient At-Home Guide for the HomeChoice/HomeChoice Pro Automated…
FDA device recall · Class III · Baxter Healthcare Renal Div
Key facts
| Recall number (Z-number) | Z-0139-06 |
|---|---|
| Recall event | 32323 |
| Product | Spanish Patient At-Home Guide for the HomeChoice/HomeChoice Pro Automated Peritoneal Dialysis Systems; Manufactured for Baxter Healthcare Corporation, Deerfield, IL 60015 U.S.A., Made in U.S.A. |
| Product code | FKX |
| Recalling firm | Baxter Healthcare Renal Div |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Jul 19, 2006 |
| 510(k) numbers | K012988 |
| FEI number | 3000210122 |
At a glance
- 1–9 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