Recall Z-0823-2015— Biomet, Inc.

Name: FDA recall Z-0823-2015
Creator: U.S. Food and Drug Administration
Published: 2014-12-02

Class II · Terminated

Class II FDA medical device recall by Biomet, Inc., initiated 2014-12-02, terminated 2015-10-27. It names one FDA 510(k) clearance: K130610. Product: Sirius Polish Cemented Stem 38C Catalog Number: 51-199335 Lot Number Identification: 141680, 180920 The Biomet's Sirius Femoral Hip Stem is a double-tapered, highly polished cemented hip stem, designed for either primary or revision surgery. A distal centralizer is provided for optimal placement within the femoral canal. The system is used with Type 1 taper modular heads and compatible acetabular shells/liners and screws to provide a total hip replacement system.. Reason: After receiving a complaint, Biomet Orthopedic Inc., conducted an investigation which determined that the following parts were mixed up prior to packaging and shipment: Sirius Polish Cemented Stem 348 Catalog Number: 51-199333, Lot Number Identification: 024320 and Sirius Polish Cemented Stem 38C, Catalog Number: 51-199335, Lot Number Identification: 141680, 180920..

Recalling firm: Biomet, Inc.
Classification: Class II
Status: Terminated
Initiated: 2014-12-02
Terminated: 2015-10-27
Firm location: Warsaw, IN, United States

510(k) clearances named in this recall

1 on FDA's record

K130610 — SIRIUS FEMORAL STEMBiomet, Inc.·cleared 2013-08-30

K-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.

Product description

Sirius Polish Cemented Stem 38C Catalog Number: 51-199335 Lot Number Identification: 141680, 180920 The Biomet's Sirius Femoral Hip Stem is a double-tapered, highly polished cemented hip stem, designed for either primary or revision surgery. A distal centralizer is provided for optimal placement within the femoral canal. The system is used with Type 1 taper modular heads and compatible acetabular shells/liners and screws to provide a total hip replacement system.

Reason for recall

After receiving a complaint, Biomet Orthopedic Inc., conducted an investigation which determined that the following parts were mixed up prior to packaging and shipment: Sirius Polish Cemented Stem 348 Catalog Number: 51-199333, Lot Number Identification: 024320 and Sirius Polish Cemented Stem 38C, Catalog Number: 51-199335, Lot Number Identification: 141680, 180920.

Data sourced from openFDA. This site is unofficial and independent of the FDA.