Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K152170 |
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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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TRULIANT Knee System including TRULIANT Tibial Inserts, also labeled as the following: a. TRULI... | 2 | 10/04/2021 | Exactech, Inc. |
Truliant Tibial Fit Tray Cemented SZ 3F / 3T, Catalog Number 02-022-45-3030 Product Usage: Knee ... | 2 | 04/23/2019 | Exactech, Inc. |
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