Medical Device Recalls
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1 result found
510(K) Number: K030853 |
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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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STERITITE Containers: STERITITE Container Kit, 1/4 size, 3" high, product code: 13902; STERITITE Min... | 3 | 12/03/2013 | Advanced Sterilization Products |
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