Venue Go Standard Carts Ref: — Class II medical device recall Z-2652-2023
Ongoing recall by GE MEDICAL SYSTEMS, ISRAEL LTD., reported 2023-10-11, distributed nationwide. Some Venue Go Standard Carts can develop an internal failure of the vertical/horizontal tilt adjustment mechan
| Recall number | Z-2652-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | GE MEDICAL SYSTEMS, ISRAEL LTD., HAIFA, N/A, Israel |
| Recall initiated | 2023-09-06 |
| Classified | 2023-09-29 |
| Reported by FDA | 2023-10-11 |
| Distributed | Nationwide (US) |
| Quantity | 5,986 devices |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00195278516510, 00840682190503 |
Product
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
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2652-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.