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FDASeptember 26, 2025device

Zimmer Biomet Dual Mobility Vivacit-E Highly Crosslinked Polyethylene, 28 mm I.D., 44 mm O.D., Size F, Bearing, Model/Catalog Number: 110031012; semi constrained hip prosthesis

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Zimmer Biomet is conducting a medical device recall for two (2) lots of the Dual Mobility Vivacit-E¿ Bearing due to a commingle. The outer package is labeled as a Size F 44 mm, however, the implant inside the package is a Size G 46 mm, and vice versa.

What to do

FDA enforcement status: Ongoing

Brands named

zimmer

UPCs

00889024572706

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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