Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K220800 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Venue Go Models: R2 (Model Number H45181VG), R3 (Model Number H45193VG), R4 (Model Number H45114VG),... | 2 | 04/11/2025 | GE Medical Systems, LLC |
| Venue Go Standard Carts Ref: (H45181VC and H45103VCW), used with Venue Go R2, R3, R4 systems R2, R3,... | 2 | 09/29/2023 | GE MEDICAL SYSTEMS, ISRAEL LTD. |
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