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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
Recall Number: Z-1979-2025
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Brand Name: Pluslife SARS-CoV-2 Card Product Name: SARS-CoV-2 Nucleic Acid Testing Card Model/Cata... 2 06/13/2025 FEI # 3037392657
Guangzhou Pluslife Biotech Co., Ltd.
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