Medical Device Recalls
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1 result found
510(K) Number: K060878 |
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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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ORCA FOAM STANDARD CUBE 10x10x10 mm, Absorbable Gelatin Sponge Hemostat, USP, REF ORCA FOAM | 2 | 09/19/2022 | GELITA MEDICAL GMBH |
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