Waldemar Link GmbH & Co. KG (Mfg Site): Medical Device Recall in 2019 - (Recall #: Z-0729-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

BiMobile UHMWPE Liner: ID-28mm/OD-54mm, Reference Number 184-260/04 The LINK BiMobile Dual Mobility System is indicated for patients with mobility-limiting diseases, fractures or defects which cannot be treated by conservative or osteosynthetic procedures. The device is intended for cemented and cementless use.

Product Classification:

Class II

Date Initiated: December 4, 2018

Date Posted: January 23, 2019

Recall Number: Z-0729-2019

Event ID: 81762

Reason for Recall:

The internal labeling included with these implants may include incorrect part numbers and could result in these incorrect labels being added to patient records.

Status: Terminated

Product Quantity: 31

Code Information:

Lot# 1707116

Distribution Pattern:

US distribution to states of: AZ, FL, GA, LA, MI, MN, TX, and WA.

Voluntary or Mandated:

Voluntary: Firm initiated