Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K083665 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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VERIFY Dual Species Self-Contained Biological Indicators, 100 per box Item Number: S3061 Intende... | 2 | 01/03/2023 | Steris Corporation |
VERIFY Dual Species Self-Contained Biological Indicators, 50 per box Item Number: S3060 Intended... | 2 | 01/03/2023 | Steris Corporation |
VERIFY Steam Test Pack (20 Tests and 20 controls) Item Number: S3069 Intended for use in install... | 2 | 01/03/2023 | Steris Corporation |
VERIFY Steam Test Pack (20 Tests and 5 controls) Item Number: S3065 Intended for use in installa... | 2 | 01/03/2023 | Steris Corporation |
VERIFY® Dual Species Self-Contained Biological Indicator, Distributed by STERIS Corporation, Mentor,... | 2 | 12/28/2013 | Steris Corporation |
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