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» Zimmer to phase out CPT device, but FDA wary of existing inventory
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Zimmer to phase out CPT device, but FDA wary of existing inventory
Sep. 17, 2024
By
Mark McCarty
The U.S. FDA reported Sept. 17 that the Zimmer Biomet Holdings Inc. CPT hip system is associated with an increased risk of thighbone fracture, a problem Zimmer acknowledged with a July 2, 2024, class II recall.
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