Medical Device Recalls
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1 result found
510(K) Number: K181362 |
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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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TEMA Axle Small, REF 1590.15.010 (additional information is pending receipt of the firm's product l... | 2 | 03/16/2023 | Limacorporate S.p.A |
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