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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K211423
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Product Description
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Recall
Class
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FDA Recall
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Rover Mobile X-ray System Model/Catalog Number: MXU-RV35 and MXU-RV71 2 04/22/2026 FEI # 3012855798
Micro-X Ltd.
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number:MXU-RV35 Product Descrip... 2 04/24/2025 FEI # 3012855798
Micro-X Ltd.
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71, MXU-RV35 Prod... 2 04/24/2025 FEI # 3012855798
Micro-X Ltd.
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV71 Product Descri... 2 04/16/2025 FEI # 3012855798
Micro-X Ltd.
Brand Name: Rover Product Name: Mobile X-ray System Model/Catalog Number: MXU-RV35 Product Descri... 2 04/16/2025 FEI # 3012855798
Micro-X Ltd.
MICRO-X Rover Mobile X-ray System, # MXU-RV19 2 12/12/2024 FEI # 3012855798
Micro-X Ltd.
MICRO-X Rover Mobile X-ray System, # MXU-RV35; MICRO-X Rover Mobile X-ray System, # MXU-RV71 2 12/12/2024 FEI # 3012855798
Micro-X Ltd.
MICRO-X Rover Mobile X-ray System, # MXU-RV35 2 12/12/2024 FEI # 3012855798
Micro-X Ltd.
MICRO-X Rover Mobile X-ray System, # MXU-RV35 2 11/27/2024 FEI # 3012855798
Micro-X Ltd.
MICRO-X ROVER MOBILE X-RAY SYSTEM, MXU-RV19 2 09/23/2022 FEI # 3012855798
Micro-X Ltd.
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