Zimmer Biomet, Inc.: Medical Device Recall in 2017 - (Recall #: Z-1024-2017)

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:

RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall +3mm Liners Size 23 item XL-108323 ArComXL MaxRom +3mm Liners Size 23 item XL-108223

Product Classification:

Class II

Date Initiated: December 19, 2016

Date Posted: January 25, 2017

Recall Number: Z-1024-2017

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: 36

Code Information:

Item XL-108323 Lot 761680 UDI (01)00880304651524(17)210713(10)761680 Item XL-108223 Lot 419460 UDI (01)00880304651494(17)210713(10)419460

Distribution Pattern:

USA (nationwide) and Internationally to ARGENTINA

Voluntary or Mandated:

Voluntary: Firm initiated