Zimmer Biomet, Inc.: Medical Device Recall in 2018 - (Recall #: Z-1008-2018)

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:

36MM COCR MODULAR HD -6MM

Product Classification:

Class II

Date Initiated: September 15, 2017

Date Posted: March 21, 2018

Recall Number: Z-1008-2018

Event ID: 79254

Reason for Recall:

One piece from a different lot mixed with lot 236840 and is incorrectly etched as -6MM offset instead of +3MM offset. As the incorrect etching and related size difference affects the functional use of this product, the affected lot is being removed from the field.

Status: Terminated

Product Quantity: 23

Code Information:

11-363660 UDI Number: (01) 00880304210509 (17) 270507 (10) 236840 Product Number: 11-363660 Lot Number: 236840

Distribution Pattern:

Outside USA

Voluntary or Mandated:

Voluntary: Firm initiated