IMPLANTCAST GMBH: Medical Device Recall in 2018 - (Recall #: Z-2517-2018)

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:

2M insert 15degree for MUTARS RS cup and LUMiC TiN orthopedic hip implant acetabular component. Size 38/39 mm REF number 02423839 Size 42/44 mm REF number 02424244 Size 44/48 mm REF number 02424448 Size 46/52 mm REF number 02424652

Product Classification:

Class II

Date Initiated: December 28, 2017

Date Posted: August 1, 2018

Recall Number: Z-2517-2018

Event ID: 80498

Reason for Recall:

Possibility that the retaining ring in the 2M inlay 15degree for MUTARS RS Cup and LUMiC TiN is incorrectly mounted.

Status: Terminated

Product Quantity: 304, 3 in US

Code Information:

Article/Batch numbers: Size 38/39 mm REF number 02423839 Batch 150201G, 1504298, 1504299, 150429C, 150429L; Size 42/44 mm REF number 02424244 Batch 1702188, 15042AF, 15042A7, 15042A6, 15042A5; Size 44/48 mm REF number 02424448 Batch 1702189, 1637108, 16141C1; Size 46/52 mm REF number 02424652 Batch 1637109, 16141C2.

Distribution Pattern:

Distribution in Europe and US states of Texas, Rhode Island and Georgia.

Voluntary or Mandated:

Voluntary: Firm initiated