Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K854902 |
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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 Indicator, Distributed by STERIS Corporation, Mentor,... | 2 | 12/28/2013 | Steris Corporation |
a. STERIS CORP Celerity Celerity 20 Sterilization Indicator Challenge Pack Steam 3 Inch Length Model... | 3 | 09/26/2022 | Mckesson Medical-Surgical Inc. Corporate Office |
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