Device recall
Z-0924-04: Medtronic Gastro pH in a Box System, Model 43A008, Catalog Number 9043A0081
FDA device recall · Class II · Medtronic Gastroenterology / Urology
Key facts
| Recall number (Z-number) | Z-0924-04 |
|---|---|
| Recall event | 28951 |
| Product | Medtronic Gastro pH in a Box System, Model 43A008, Catalog Number 9043A0081 |
| Product code | FFX |
| Recalling firm | Medtronic Gastroenterology / Urology |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 21, 2005 |
| 510(k) numbers | K981733 |
| FEI number | 1000135098 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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