GE Medical Systems recalls Venue Go Standard Carts (H45181VC, H45103VCW) made 2022-08 or earlier that may detach from cart, causing fall risk. Affected users should contact GE for details.
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.
GE Medical Systems recalls Venue Go Standard Carts with specific model numbers that were made in August 2022 or earlier. These carts can fail internally, causing the medical imaging system to detach and fall, which poses a risk of injury.
The tilt adjustment mechanism in some carts can fail internally, causing the medical imaging system to detach from the cart. If the system falls, it could cause injury to the user or patient.
Medical professionals using GE Venue Go R2, R3, or R4 systems with the recalled carts. Those who use the carts for pulsed Doppler imaging are most at risk.
Check for model numbers H45181VC or H45103VCW on the cart. These carts were made in August 2022 or earlier and used with GE Venue Go R2, R3, or R4 systems.
Identify the cart model number on the device to see if it matches H45181VC or H45103VCW.
Reach out to GE Medical Systems for specific instructions on how to address the issue.
The affected model numbers are H45181VC and H45103VCW.
These carts were manufactured in August 2022 or earlier.
The tilt adjustment mechanism can fail internally, causing the Venue Go system to detach from the cart and fall.
We’ve drafted a message you can send GE Medical Systems to request your refund or repair — edit it as you like.
Subject: Recall Z-2652-2023 — GE Medical Systems GE Medical Systems Hello, I own a GE Medical Systems that is covered by recall Z-2652-2023 from GE Medical Systems. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
