Waldemar Link GmbH & Co. KG (Mfg Site): Medical Device Recall in 2024 - (Recall #: Z-1219-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

LINK BiMobile Dual Mobility System E-Poly Liner for 28mm Head, 70mm Shell- Indicated for patients with mobility-limiting diseases, fractures or defects of the hip joint or proximal femur. Item Number: 184-280/12

Product Classification:

Class II

Date Initiated: January 22, 2024

Date Posted: March 6, 2024

Recall Number: Z-1219-2024

Event ID: 93944

Reason for Recall:

Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery

Status: Ongoing

Product Quantity:

Code Information:

UDI-DI: 04026575230747 Lot Numbers: 2334253, 2325426

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of IL, IN, FL, WA and the countries of Germany, Switzerland.

Voluntary or Mandated:

Voluntary: Firm initiated