Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1025-2017)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2017.

Data Source: FDA.

Product Description:

Active Articulation ArComXL Polyethylene Bearings Active Articulation ArComXL Bearings item XL-200152

Product Classification:

Class II

Date Initiated: December 19, 2016

Date Posted: January 25, 2017

Recall Number: Z-1025-2017

Event ID: 75970

Reason for Recall:

Product complaints indicated that the part and lot numbers on the packaging differed from the physical product inside the packaging. Risk of delay in surgery.

Status: Terminated

Product Quantity: 19

Code Information:

Item XL-200152 Lot 339260 UDI (01)00880304491366(17)210713(10)339260

Distribution Pattern:

USA (nationwide) and Internationally to ARGENTINA

Voluntary or Mandated:

Voluntary: Firm initiated