Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-2177-2018)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

Biomet Modular Primary Tibial Tray Implants; Modular Interlok Primary Tray (size 75 mm); Item No. 141215; UDI: (01) 00880304005310 (17) 280306 (10) 385340 Product is used in Total Knee Arthroplasty

Product Classification:

Class II

Date Initiated: May 18, 2018

Date Posted: June 20, 2018

Recall Number: Z-2177-2018

Event ID: 80185

Reason for Recall:

One lot of 75mm tibial tray is potentially etched and labeled as a 79 mm tibial tray. This may lead to delay in surgery, or immediate revision surgery to remove an incorrectly sized tibial component after it has been cemented.

Status: Terminated

Product Quantity: 16

Code Information:

Lot 385340 UDI: (01) 00880304005310 (17) 280306 (10) 385340

Distribution Pattern:

US Distribution to the states of : FL, GA, IN, MA, NM, UT, and WI. Foreign distribution to Canada and Mexico

Voluntary or Mandated:

Voluntary: Firm initiated