Device recall
Z-0936-2018: Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an…
FDA device recall · Class II · Medtronic Minimally Invasive Therapies Group
Key facts
| Recall number (Z-number) | Z-0936-2018 |
|---|---|
| Recall event | 79352 |
| Product | Argyle Suction Tubing (Product # 8888301515) Argyle Suction Tubing is an extruded tube used as an extension for different types of devices in an operating room, bonded with 2 female sure grip connectors at each end of the tube to facilitate the plug/ insertion of the device and also includes a male… |
| Product code | GAZ |
| Recalling firm | Medtronic Minimally Invasive Therapies Group |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 26, 2020 |
| FEI number | 1282497 |
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