Device recall
Z-0392-06: Medtronic Slimline Single-Use Internal Reference pH Catheter for…
FDA device recall · Class III · Medtronic Gastroenterology / Urology
Key facts
| Recall number (Z-number) | Z-0392-06 |
|---|---|
| Recall event | 34246 |
| Product | Medtronic Slimline Single-Use Internal Reference pH Catheter for Gastroesophageal pH measurements. Models 9012P3101, 9012P3111, 9012P3121, 9012P3131 and 9012P3141. Distributed by / Medtronic Inc. 710 Medtronic Parkway NE, Minneapolis, MN 55432-5604 USA |
| Product code | FFT |
| Recalling firm | Medtronic Gastroenterology / Urology |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Dec 21, 2006 |
| FEI number | 1000135098 |
At a glance
- None 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