HAIFA, N/A, Israel
GE MEDICAL SYSTEMS, ISRAEL LTD. recalls
1 recall recorded since 2018, most recently on 6 September 2023. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 6 September 2023
- Reason
- 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.
- Distribution
- Worldwide distribution - US Nationwide distribution including government and military distribution as well as PR.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2652-2023
- 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
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.