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Serious recall: Injury is possible or has been reported. Take action promptly.

GE MEDICAL SYSTEMS, ISRAEL LTD. 2023-10-11 Health serious FDA
Health · FDA · Recall #FDA-Z-2652-2023

Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4… Recall

Issued October 11, 2023 · GE MEDICAL SYSTEMS, ISRAEL LTD.

In October 2023, GE MEDICAL SYSTEMS, ISRAEL LTD. recalled the Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4…, a serious health recall reported by the FDA.

Compiled by Maya Ellison, RecallCheckr

What this means for you

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.

What you should do

  1. 1 Stop using Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4… right away.
  2. 2 Set it aside where it won't be used by mistake.
  3. 3 Contact GE MEDICAL SYSTEMS, ISRAEL LTD. to arrange your voluntary. See the official notice below for contact details.
  4. 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):

Recall details

Brand
GE MEDICAL SYSTEMS, ISRAEL LTD.
Category
Health
Recall date
October 11, 2023
Units affected
Not reported
Sold at
Worldwide distribution - US Nationwide distribution including government and military distribution as well as PR.
Recall number
FDA-Z-2652-2023
Made in
Israel
Issuing agency
FDA

In context

  • GE MEDICAL SYSTEMS, ISRAEL LTD. has 1 recall in our database.
  • We're tracking 3,576 Health recalls in our database.
  • This is the 903rd Health recall we've logged in 2023.
Read the official FDA notice

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