Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K020430 |
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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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NextStep Retrograde Replacement Hub Set - Product Usage: is indicated for use in the replacement of ... | 2 | 08/13/2020 | Arrow International Inc |
Cannon II Plus Replacement Hub Set - Product Usage: is indicated for use in the replacement of a Can... | 2 | 08/13/2020 | Arrow International Inc |
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