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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K012391
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Recall
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FDA Recall
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Oridion Surestream CO2 Sampling Lines- SureLine Adult Part Number: 010976-03 Product Usage: T... 2 03/30/2012 FEI # 3001227743
Oridion Medical 1987 Ltd.
Oridion Surestream CO2 Sampling Lines- Smart SureLine Plus O2 adult Part Number: 010981-03 Prod... 2 03/30/2012 FEI # 3001227743
Oridion Medical 1987 Ltd.
Oridion CO2 sampling lines and water traps under the label: Surestream CO2 Sampling Lines: SureLin... 2 03/29/2012 FEI # 3001227743
Oridion Medical 1987 Ltd.
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