Device recall
Z-1792-2020: 0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. REF/UDI…
FDA device recall · Class I · Argon Medical Devices, Inc
Key facts
| Recall number (Z-number) | Z-1792-2020 |
|---|---|
| Recall event | 85398 |
| Product | 0.035"(.89mm)x150 cm guidewire. Model 114135150. Soft Tip 3.5cm. REF/UDI: 114135150/(01)20886333008074. RxOnly.STERILE EO |
| Product code | DQX |
| Recalling firm | Argon Medical Devices, Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Apr 1, 2024 |
| 510(k) numbers | K160785 |
| FEI number | 1625425 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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