Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0630-2019)

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:

NexGen¿ Complete Knee Solution Femoral Augment Block Distal only, 15mm, Size E with Screw Item Number: 00599003523 NexGen Distal Femoral Augment Block is used when femoral components can neither be downsized nor can be distally augmented by increasing the thickness of the cement mantle.

Product Classification:

Class II

Date Initiated: October 31, 2018

Date Posted: December 26, 2018

Recall Number: Z-0630-2019

Event ID: 81604

Reason for Recall:

Screw is missing from the package

Status: Terminated

Product Quantity: 19 units

Code Information:

Lot Number: 62925336 UDI Number: (01)00889024224131(17)250228(10)62925336

Distribution Pattern:

Worldwide Distribution: US (nationwide) to states of: OH, FL, NJ, NY, OH, PA, TX, WV and to countries of: CANADA, AUSTRALIA, JAPAN, GERMANY, and NETHERLANDS.

Voluntary or Mandated:

Voluntary: Firm initiated