Zimmer, Inc.: Medical Device Recall in 2013 - (Recall #: Z-1376-2013)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

NEXGEN Complete Knee Solution Monoblock Tibial Drill with stop 10.7 mm. Used to prepare cylindrical holes in the native tibia.

Product Classification:

Class II

Date Initiated: March 27, 2013

Date Posted: June 5, 2013

Recall Number: Z-1376-2013

Event ID: 65042

Reason for Recall:

Zimmer is initiating a lot specific recall of the Trabecular Metal" Tibia Stop Drill due to the potential of the outside diameter being oversized. As a result, there is a potential for the drill to not pass through the applicable drill guide.

Status: Terminated

Product Quantity: 69 units

Code Information:

Part No. 00-5887-052-00; lots 62181290 and 62183430

Distribution Pattern:

Nationwide Distribution.

Voluntary or Mandated:

Voluntary: Firm initiated