Medical Device Recalls
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1 result found
510(K) Number: K964056 |
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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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Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised patients, particularly in th... | 1 | 10/18/2016 | Teleflex Medical |
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