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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K023290
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Product Description
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Recall
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FDA Recall
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STERRAD 50, Product Code 10114. The STERRAD Cassettes are used on STERRAD Sterilization System wh... 2 12/22/2014 FEI # 3003662624
Advanced Sterilization Products
STERRAD 100S, Product Code 10113. The STERRAD Cassettes are used on STERRAD Sterilization System ... 2 12/22/2014 FEI # 3003662624
Advanced Sterilization Products
STERRAD 50 Sterilization System, Product Code: 10050 The STERRAD 50 Sterilization System is a gener... 2 01/14/2014 FEI # 3003662624
Advanced Sterilization Products
STERRAD 100S Sterilization System, Product Code: 10101 The STERRAD 100S Sterilization System is a g... 2 01/14/2014 FEI # 3003662624
Advanced Sterilization Products
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