Biomet, Inc.: Medical Device Recall in 2016 - (Recall #: Z-0650-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

Biomet Integral Centralizer Hip System, Lateralized Femoral Stem (Co-Cr-Mo), 9mm, 11mm, 13mm, 15mm, and 17mm

Product Classification:

Class II

Date Initiated: November 17, 2015

Date Posted: January 20, 2016

Recall Number: Z-0650-2016

Event ID: 72521

Reason for Recall:

PMMA is listed as a material on the label but the product does not contain PMMA.

Status: Terminated

Product Quantity: 21

Code Information:

Part #11-162709 9mm Lots: 329750, 404380, 487400, 767120, 951680 Part # 11-162711 11mm Lots: 329760, 505030, 505050 Part # 11-162713 13mm Lots: 837750, 977460 Part # 11-162715 15mm 772410, 837780, 897070, 951810 Part # 11-162717 17mm Lots: 311410, 410500, 535530, 712800, 728080, 829580

Distribution Pattern:

Worldwide distribution. US nationwide including IA, UT, MN, PA, MO, OK, IL, OH, and WA; CANADA, and NETHERLANDS

Voluntary or Mandated:

Voluntary: Firm initiated