Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K953653 |
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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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SPII Model Lubinus, Hip Prosthesis Stem Standard Neck, cemented | 2 | 03/14/2024 | Waldemar Link GmbH & Co. KG (Mfg Site) |
SPII Model Lubinus, Long Stem Prosthesis XL Neck, cemented | 2 | 03/14/2024 | Waldemar Link GmbH & Co. KG (Mfg Site) |
SPII Model Lubinus, Long Stem Prosthesis Standard Neck, cemented | 2 | 03/14/2024 | Waldemar Link GmbH & Co. KG (Mfg Site) |
SPII Model Lubinus, Hip Prosthesis Stem XL Neck, cemented | 2 | 03/14/2024 | Waldemar Link GmbH & Co. KG (Mfg Site) |
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