Medical Device Recalls
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1 to 5 of 5 Results
510(K) Number: K181630 |
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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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'n'-Hole Post which is a component of the Revolution External Fixation System Catalog Numbers: 1... | 2 | 06/09/2023 | New Standard Device Inc |
Metalogix Self-Drill Half-Pin, a component of the Revolution External Fixation System. Orthopedic. ... | 2 | 08/29/2022 | New Standard Device Inc |
Metalogix Slotted 90 Tubular Wrench x 10mm REF 900104 LOT A29618A | 2 | 06/21/2022 | New Standard Device Inc |
1.8mm Truss Wire, REF: 900217, a Component of Metalogix Revolution External Plating System | 2 | 06/03/2022 | New Standard Device Inc |
Various Hip Joint Replacement Systems, Item Nos. 00151504232 00151504432 00151504636 00151504836 ... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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