Reported Oct 11, 2023 · Ongoing
Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems;…
Ge Medical Systems, Israel Ltd.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: GE MEDICAL SYSTEMS, ISRAEL LTD. · Nativ Haa??or Street no. 1 · HAIFA, N/A · N/A
Is this the product you have?
- Venue Go Standard Carts Ref
(H45181VC and H45103VCW)used with Venue Go R2R3R4 systems R2R3and R4 systemspulsed doppler imaging system
- Lot codes and dates
- Venue Go Standard Carts
- Ref(H45181VC and H45103VCW) used with Venue Go R2, R3, R4 systems R2, R3, and R4 systems (GTIN 0084068213884, 00840682190503, and 00195278516510) that were manufactured 2022-08 and before
- Amount recalled
- 5986 devices
Where it was sold
- Nationwide
- PR
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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