Medical Device Recalls
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1 result found
Recall Number: Z-2622-2025 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BeneVision N1 Patient Monitor (N1). Part Numbers: 6660E-PA00017, 6660E-PA00014, 6660E-PA00012, 6660E... | 2 | 09/25/2025 |
FEI # 2221819 Mindray DS USA, Inc. dba Mindray North America |
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