Device recall
Z-0830-06: Medtronic Zinetics 24ME Multi-Use External Reference pH Catheter. For…
FDA device recall · Class II · Medtronic Gastroenterology / Urology
Key facts
| Recall number (Z-number) | Z-0830-06 |
|---|---|
| Recall event | 34535 |
| Product | Medtronic Zinetics 24ME Multi-Use External Reference pH Catheter. For Gastroesophageal pH Measurements. Catalog number 9012P2121. Distributed by Medtronic, Inc., 710 Medtronic Parkway NE, Minneapolis, MN 55432-5604, USA. |
| Product code | FFT |
| Recalling firm | Medtronic Gastroenterology / Urology |
| Recall class | Class II |
| 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