Device recall
Z-2652-2023: Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2…
FDA device recall · Class II · GE MEDICAL SYSTEMS, ISRAEL LTD.
Key facts
| Recall number (Z-number) | Z-2652-2023 |
|---|---|
| Recall event | 93069 |
| Product | Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems; pulsed doppler imaging system |
| Product code | IYN |
| Recalling firm | GE MEDICAL SYSTEMS, ISRAEL LTD. |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K183362, K202233, K220800 |
| FEI number | 3002973981 |
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