Medical Device Recalls
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1 to 6 of 6 Results
510(K) Number: K162024 |
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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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AltiVate Anatomic Shoulder System for the following Part Numbers: 1. Part # 520-08-00, Rev. C., 2... | 2 | 08/23/2021 | Encore Medical, LP |
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 42mm, REF 804-07-420 Product Us... | 2 | 03/28/2018 | Encore Medical, Lp |
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 50mm, REF 804-07-500 Product Us... | 2 | 03/28/2018 | Encore Medical, Lp |
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 54mm, REF 804-07-540 Produc... | 2 | 03/28/2018 | Encore Medical, Lp |
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 38mm, REF 804-07-380 Product Us... | 2 | 03/28/2018 | Encore Medical, Lp |
Altivate Anatomic(TM) INSTRUMENTATION, PEGGED GLENOID TRIAL, SIZE 46mm, REF 804-07-460 Product Us... | 2 | 03/28/2018 | Encore Medical, Lp |
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