Medical Device Recalls
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1 result found
510(K) Number: K190535 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients wi... | 2 | 02/29/2024 |
FEI # 3003386935 Waldemar Link GmbH & Co. KG (Mfg Site) |
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