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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 37 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
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Z-0031-2019 - Capnostream20 (US) M W/PRINTER TO MASIMO, Part Number CS08751 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0035-2019 - Capnostream20 (US) M W/PRINTER REFURBISHED, Part Number CS78659 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0030-2019 - Capnostream20 (US) M TO MASIMO, Part Number CS08750 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0053-2019 - Capnostream20 (INTL) N W/PRINTER REFURBISHED, CS78658 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0051-2019 - Capnostream20 (INTL) N REFURBISHED, CS78652 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0044-2019 - Capnostream20 (INTL) M, CS08654 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0047-2019 - Capnostream20 (INTL) M W/PRINTER, CS08660 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0054-2019 - Capnostream20 (INTL) M W/PRINTER REFURBISHED, CS78660 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0052-2019 - Capnostream20 (INTL) M REFURBISHED, CS78654 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
Z-0021-2019 - CAPNOSTREAM 20P (US) N, Part Number CS08651-01 2 10/03/2018 FEI # 3001227743
Oridion Medical 1987 Ltd.
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