Waldemar Link GmbH & Co. KG (Corp. Hq.): Medical Device Recall in 2013 - (Recall #: Z-2071-2013)

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:

TRIAL STEM for MP(R) RECONSTRUCTION PROTHESIS, REF 99-0143/20, Stem size 04, prox. Stem dia. 20 mm, Length 250 mm, WALDEMAR LINK GmbH & CoKG, Barkhausenweg 10 . D . 22339 Hamburg

Product Classification:

Class II

Date Initiated: July 16, 2013

Date Posted: September 4, 2013

Recall Number: Z-2071-2013

Event ID: 65800

Reason for Recall:

The trial stems were manufactured using the wrong design.

Status: Terminated

Product Quantity: 5 units

Code Information:

Lots: B209033, B225119

Distribution Pattern:

US Distribution to the state of Tennessee only.

Voluntary or Mandated:

Voluntary: Firm initiated