Zimmer, Inc.: Medical Device Recall in 2025 - (Recall #: Z-0418-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 26, 2025

Date Posted: November 12, 2025

Recall Number: Z-0418-2026

Event ID: 97765

Reason for Recall:

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.

Status: Ongoing

Product Quantity: 72 units

Code Information:

UDI (01)00889024572706(17)300406(10)67160447; Lot Number 67160447

Distribution Pattern:

US: OH, GA, WI, NE, IA, IL, CA, NY, MD, NC, PA, AL, TN, MI, WA, FL, TX, KS, NM, AZ, and CANADA, AUSTRALIA, NETHERLANDS

Voluntary or Mandated:

Voluntary: Firm initiated