Drug recall
Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4…
FDA recall event 93069 · Class II · GE MEDICAL SYSTEMS, ISRAEL LTD.
Key facts
| Event ID | 93069 |
|---|---|
| Recall numbers | Z-2652-2023 |
| Recalling firm | GE MEDICAL SYSTEMS, ISRAEL LTD. |
| Product type | Devices |
| Products | 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 |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechanism which can result in the Venue Go system detaching from the cart and falling. |
| Initiation date | Sep 6, 2023 |
| Report date | Oct 11, 2023 |
| City | HAIFA |
| Country | Israel |
| FEI number | 3002973981 |
At a glance
- 1–9 Products in this recall
- None FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: