Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K961763 |
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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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Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 10 cm Infusion Pattern, Catalog No./REF 1240... | 2 | 08/18/2014 | Angiodynamics, Inc. |
Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 40 cm Infusion Pattern, Catalog No./REF 1240... | 2 | 08/18/2014 | Angiodynamics, Inc. |
Uni*Fuse INFUSION SYSTEM WITH COOPER WIRE, 5F x 90 cm x 30 cm Infusion Pattern, Catalog No./REF 1240... | 2 | 08/18/2014 | Angiodynamics, Inc. |
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