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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 11 Results
510(K) Number: K181467
 
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Product Description
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Recall
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FDA Recall
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Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLin... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: FilterLin... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Filter Li... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Airway Ad... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: OmniVentL... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstre... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstre... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstre... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstre... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
Microstream Instructions for Use and Part Number used with - Product Description, REF: Microstre... 2 03/17/2025 FEI # 3001227743
Oridion Medical 1987 Ltd.
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