Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K023880 |
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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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Steerable Coronary Sinus Catheter, Model SCS01, 9 Fr x 20.4", Sterile R, Edwards Lifesciences Port A... | 2 | 07/11/2011 | Edwards Lifesciences, LLC |
Steerable Coronary Sinus Catheter Kit, REF SCS01, 9 Fr x 20.4", Contains Phthalates, Sterile EO, Edw... | 2 | 01/28/2011 | Edwards Lifesciences Llc |
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